Please choose an event type to view the corresponding MedsFacts report:

PAIN ( 3198 FDA reports)
DRUG INEFFECTIVE ( 2403 FDA reports)
NAUSEA ( 2391 FDA reports)
FATIGUE ( 2006 FDA reports)
DIZZINESS ( 1926 FDA reports)
DYSPNOEA ( 1914 FDA reports)
HEADACHE ( 1817 FDA reports)
ANXIETY ( 1799 FDA reports)
DIARRHOEA ( 1693 FDA reports)
FALL ( 1691 FDA reports)
ASTHENIA ( 1651 FDA reports)
VOMITING ( 1602 FDA reports)
PAIN IN EXTREMITY ( 1498 FDA reports)
DEPRESSION ( 1470 FDA reports)
BACK PAIN ( 1418 FDA reports)
PYREXIA ( 1399 FDA reports)
OEDEMA PERIPHERAL ( 1374 FDA reports)
PNEUMONIA ( 1296 FDA reports)
ARTHRALGIA ( 1227 FDA reports)
SOMNOLENCE ( 1173 FDA reports)
HYPOAESTHESIA ( 1158 FDA reports)
INSOMNIA ( 1153 FDA reports)
CONFUSIONAL STATE ( 1107 FDA reports)
ANAEMIA ( 1089 FDA reports)
CHEST PAIN ( 1088 FDA reports)
HYPERTENSION ( 1051 FDA reports)
MALAISE ( 1046 FDA reports)
ABDOMINAL PAIN ( 1034 FDA reports)
CONSTIPATION ( 984 FDA reports)
GAIT DISTURBANCE ( 950 FDA reports)
WEIGHT INCREASED ( 931 FDA reports)
WEIGHT DECREASED ( 930 FDA reports)
CONVULSION ( 930 FDA reports)
DRUG INTERACTION ( 927 FDA reports)
COMPLETED SUICIDE ( 924 FDA reports)
HYPOTENSION ( 908 FDA reports)
PARAESTHESIA ( 903 FDA reports)
TREMOR ( 896 FDA reports)
NEUROPATHY PERIPHERAL ( 858 FDA reports)
MUSCLE SPASMS ( 802 FDA reports)
RASH ( 802 FDA reports)
URINARY TRACT INFECTION ( 802 FDA reports)
FEELING ABNORMAL ( 796 FDA reports)
DEATH ( 790 FDA reports)
RENAL FAILURE ACUTE ( 790 FDA reports)
DEHYDRATION ( 777 FDA reports)
VISION BLURRED ( 752 FDA reports)
INJURY ( 749 FDA reports)
LOSS OF CONSCIOUSNESS ( 732 FDA reports)
MUSCULAR WEAKNESS ( 707 FDA reports)
PRURITUS ( 695 FDA reports)
OSTEONECROSIS OF JAW ( 693 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 686 FDA reports)
DECREASED APPETITE ( 653 FDA reports)
COUGH ( 650 FDA reports)
BLOOD GLUCOSE INCREASED ( 648 FDA reports)
CONDITION AGGRAVATED ( 648 FDA reports)
MEMORY IMPAIRMENT ( 635 FDA reports)
RENAL FAILURE ( 635 FDA reports)
SUICIDAL IDEATION ( 616 FDA reports)
EMOTIONAL DISTRESS ( 609 FDA reports)
DYSPHAGIA ( 608 FDA reports)
MYOCARDIAL INFARCTION ( 605 FDA reports)
DIABETES MELLITUS ( 602 FDA reports)
MYALGIA ( 599 FDA reports)
ABDOMINAL PAIN UPPER ( 579 FDA reports)
HYPERHIDROSIS ( 572 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 559 FDA reports)
BONE DISORDER ( 555 FDA reports)
CEREBROVASCULAR ACCIDENT ( 551 FDA reports)
OSTEOARTHRITIS ( 549 FDA reports)
THROMBOCYTOPENIA ( 549 FDA reports)
BALANCE DISORDER ( 542 FDA reports)
SEPSIS ( 533 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 525 FDA reports)
SYNCOPE ( 523 FDA reports)
INFECTION ( 511 FDA reports)
CARDIAC ARREST ( 506 FDA reports)
OVERDOSE ( 498 FDA reports)
CONTUSION ( 496 FDA reports)
AMNESIA ( 492 FDA reports)
PAIN IN JAW ( 492 FDA reports)
ERYTHEMA ( 482 FDA reports)
HAEMOGLOBIN DECREASED ( 482 FDA reports)
CELLULITIS ( 478 FDA reports)
NEUTROPENIA ( 470 FDA reports)
PLEURAL EFFUSION ( 459 FDA reports)
CHILLS ( 451 FDA reports)
AGITATION ( 443 FDA reports)
OSTEOMYELITIS ( 440 FDA reports)
PULMONARY EMBOLISM ( 437 FDA reports)
MENTAL STATUS CHANGES ( 434 FDA reports)
BRONCHITIS ( 431 FDA reports)
BLOOD PRESSURE INCREASED ( 428 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 421 FDA reports)
DEEP VEIN THROMBOSIS ( 419 FDA reports)
LETHARGY ( 417 FDA reports)
OEDEMA ( 405 FDA reports)
SPINAL OSTEOARTHRITIS ( 402 FDA reports)
NECK PAIN ( 400 FDA reports)
PANCYTOPENIA ( 399 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 399 FDA reports)
BLOOD CREATININE INCREASED ( 392 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 392 FDA reports)
JOINT SWELLING ( 392 FDA reports)
HALLUCINATION ( 389 FDA reports)
DRY MOUTH ( 384 FDA reports)
INJECTION SITE PAIN ( 380 FDA reports)
HYPOKALAEMIA ( 378 FDA reports)
ARTHRITIS ( 375 FDA reports)
SINUSITIS ( 368 FDA reports)
DYSPEPSIA ( 366 FDA reports)
NEURALGIA ( 364 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 363 FDA reports)
ABDOMINAL DISCOMFORT ( 360 FDA reports)
BONE PAIN ( 360 FDA reports)
ATRIAL FIBRILLATION ( 358 FDA reports)
DYSKINESIA ( 354 FDA reports)
INFLUENZA LIKE ILLNESS ( 354 FDA reports)
DRUG TOXICITY ( 352 FDA reports)
RESPIRATORY FAILURE ( 350 FDA reports)
SWELLING ( 347 FDA reports)
HERPES ZOSTER ( 345 FDA reports)
MUSCULOSKELETAL PAIN ( 345 FDA reports)
TYPE 2 DIABETES MELLITUS ( 344 FDA reports)
DISORIENTATION ( 341 FDA reports)
IMPAIRED HEALING ( 339 FDA reports)
VISUAL IMPAIRMENT ( 337 FDA reports)
CHEST DISCOMFORT ( 336 FDA reports)
HYPERSENSITIVITY ( 336 FDA reports)
SPEECH DISORDER ( 334 FDA reports)
ANHEDONIA ( 333 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 331 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 330 FDA reports)
DYSARTHRIA ( 328 FDA reports)
RESPIRATORY ARREST ( 328 FDA reports)
ATELECTASIS ( 327 FDA reports)
PALPITATIONS ( 326 FDA reports)
PLATELET COUNT DECREASED ( 326 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 326 FDA reports)
TOOTH EXTRACTION ( 325 FDA reports)
FLUSHING ( 324 FDA reports)
TACHYCARDIA ( 323 FDA reports)
DEFORMITY ( 317 FDA reports)
BURNING SENSATION ( 316 FDA reports)
OSTEONECROSIS ( 313 FDA reports)
ALOPECIA ( 311 FDA reports)
CATARACT ( 311 FDA reports)
SWELLING FACE ( 310 FDA reports)
CHOLELITHIASIS ( 307 FDA reports)
TOOTHACHE ( 305 FDA reports)
SUICIDE ATTEMPT ( 304 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 301 FDA reports)
STRESS ( 300 FDA reports)
INJECTION SITE ERYTHEMA ( 298 FDA reports)
HAEMORRHOIDS ( 296 FDA reports)
HYPOPHAGIA ( 296 FDA reports)
PULMONARY OEDEMA ( 292 FDA reports)
NERVOUSNESS ( 291 FDA reports)
CORONARY ARTERY DISEASE ( 290 FDA reports)
GASTRITIS ( 287 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 286 FDA reports)
OSTEOPOROSIS ( 284 FDA reports)
DRUG DOSE OMISSION ( 282 FDA reports)
MULTIPLE MYELOMA ( 282 FDA reports)
MIGRAINE ( 281 FDA reports)
URTICARIA ( 281 FDA reports)
URINARY INCONTINENCE ( 280 FDA reports)
BLOOD PRESSURE DECREASED ( 280 FDA reports)
HIATUS HERNIA ( 280 FDA reports)
ASTHMA ( 279 FDA reports)
DRUG EFFECT DECREASED ( 279 FDA reports)
DISTURBANCE IN ATTENTION ( 277 FDA reports)
HYPONATRAEMIA ( 274 FDA reports)
RENAL IMPAIRMENT ( 274 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 274 FDA reports)
SLEEP DISORDER ( 272 FDA reports)
COGNITIVE DISORDER ( 272 FDA reports)
OSTEOPENIA ( 269 FDA reports)
RHABDOMYOLYSIS ( 269 FDA reports)
METASTASES TO BONE ( 267 FDA reports)
INCORRECT DOSE ADMINISTERED ( 266 FDA reports)
ABDOMINAL DISTENSION ( 265 FDA reports)
RENAL FAILURE CHRONIC ( 265 FDA reports)
DYSURIA ( 262 FDA reports)
CARDIOMEGALY ( 261 FDA reports)
ABASIA ( 260 FDA reports)
HEART RATE INCREASED ( 260 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 259 FDA reports)
LEUKOPENIA ( 259 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 258 FDA reports)
MYOCLONUS ( 258 FDA reports)
DENTAL CARIES ( 257 FDA reports)
SLEEP APNOEA SYNDROME ( 257 FDA reports)
MOBILITY DECREASED ( 255 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 254 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 251 FDA reports)
MENTAL DISORDER ( 251 FDA reports)
MITRAL VALVE INCOMPETENCE ( 250 FDA reports)
NEOPLASM MALIGNANT ( 248 FDA reports)
CARDIO-RESPIRATORY ARREST ( 247 FDA reports)
STAPHYLOCOCCAL INFECTION ( 245 FDA reports)
URINARY RETENTION ( 244 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 243 FDA reports)
UNRESPONSIVE TO STIMULI ( 242 FDA reports)
VERTIGO ( 242 FDA reports)
EXOSTOSIS ( 241 FDA reports)
HYPERGLYCAEMIA ( 241 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 240 FDA reports)
COMA ( 240 FDA reports)
HYPERKALAEMIA ( 238 FDA reports)
HYPOGLYCAEMIA ( 238 FDA reports)
HYPERLIPIDAEMIA ( 237 FDA reports)
VISUAL ACUITY REDUCED ( 237 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 235 FDA reports)
DYSGEUSIA ( 235 FDA reports)
DIVERTICULUM ( 234 FDA reports)
LYMPHADENOPATHY ( 234 FDA reports)
MULTIPLE SCLEROSIS ( 233 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 233 FDA reports)
AGGRESSION ( 232 FDA reports)
RECTAL HAEMORRHAGE ( 231 FDA reports)
CARDIAC DISORDER ( 230 FDA reports)
FEBRILE NEUTROPENIA ( 228 FDA reports)
NASOPHARYNGITIS ( 228 FDA reports)
SURGERY ( 227 FDA reports)
HAEMATOCHEZIA ( 226 FDA reports)
PANCREATITIS ( 225 FDA reports)
EPISTAXIS ( 224 FDA reports)
SEDATION ( 223 FDA reports)
OFF LABEL USE ( 222 FDA reports)
PRODUCT QUALITY ISSUE ( 222 FDA reports)
DISEASE PROGRESSION ( 221 FDA reports)
MUSCLE TWITCHING ( 218 FDA reports)
BRADYCARDIA ( 216 FDA reports)
DYSPNOEA EXERTIONAL ( 212 FDA reports)
HYPOXIA ( 212 FDA reports)
POLLAKIURIA ( 211 FDA reports)
WHEEZING ( 211 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 210 FDA reports)
DEPRESSED MOOD ( 210 FDA reports)
ABNORMAL BEHAVIOUR ( 209 FDA reports)
HAEMORRHAGE ( 209 FDA reports)
INTENTIONAL DRUG MISUSE ( 209 FDA reports)
RESPIRATORY DISTRESS ( 209 FDA reports)
UNEVALUABLE EVENT ( 207 FDA reports)
CARPAL TUNNEL SYNDROME ( 207 FDA reports)
DECREASED INTEREST ( 207 FDA reports)
INFLUENZA ( 207 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 207 FDA reports)
COORDINATION ABNORMAL ( 206 FDA reports)
ROAD TRAFFIC ACCIDENT ( 206 FDA reports)
SCAR ( 205 FDA reports)
BLOOD GLUCOSE DECREASED ( 205 FDA reports)
EYE PAIN ( 205 FDA reports)
OROPHARYNGEAL PAIN ( 205 FDA reports)
DRUG HYPERSENSITIVITY ( 204 FDA reports)
DIPLOPIA ( 203 FDA reports)
IRRITABILITY ( 203 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 202 FDA reports)
RESTLESSNESS ( 202 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 201 FDA reports)
SKIN ULCER ( 200 FDA reports)
THROMBOSIS ( 200 FDA reports)
WITHDRAWAL SYNDROME ( 199 FDA reports)
BLISTER ( 199 FDA reports)
INJECTION SITE HAEMATOMA ( 199 FDA reports)
CYSTITIS ( 198 FDA reports)
HAEMATOCRIT DECREASED ( 198 FDA reports)
DRUG DEPENDENCE ( 197 FDA reports)
BLOOD POTASSIUM DECREASED ( 195 FDA reports)
ANGER ( 192 FDA reports)
LUNG INFILTRATION ( 192 FDA reports)
DELIRIUM ( 190 FDA reports)
DISCOMFORT ( 190 FDA reports)
BLOOD UREA INCREASED ( 187 FDA reports)
FIBROMYALGIA ( 185 FDA reports)
ORAL PAIN ( 185 FDA reports)
RENAL CYST ( 185 FDA reports)
OBESITY ( 184 FDA reports)
ECONOMIC PROBLEM ( 182 FDA reports)
CARDIAC FAILURE ( 181 FDA reports)
DIABETIC NEUROPATHY ( 179 FDA reports)
TREATMENT NONCOMPLIANCE ( 179 FDA reports)
RIB FRACTURE ( 178 FDA reports)
STOMATITIS ( 177 FDA reports)
DYSPHONIA ( 177 FDA reports)
FEELING HOT ( 177 FDA reports)
ORAL DISORDER ( 177 FDA reports)
ANGINA PECTORIS ( 176 FDA reports)
HOT FLUSH ( 176 FDA reports)
NEPHROLITHIASIS ( 176 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 175 FDA reports)
DRY EYE ( 174 FDA reports)
HAEMATEMESIS ( 174 FDA reports)
HIP FRACTURE ( 174 FDA reports)
DYSSTASIA ( 173 FDA reports)
FLATULENCE ( 173 FDA reports)
TOOTH LOSS ( 172 FDA reports)
TOOTH DISORDER ( 171 FDA reports)
BONE LESION ( 171 FDA reports)
NERVOUS SYSTEM DISORDER ( 170 FDA reports)
PANIC ATTACK ( 169 FDA reports)
SKIN DISCOLOURATION ( 169 FDA reports)
DRUG ABUSE ( 168 FDA reports)
HEPATIC ENZYME INCREASED ( 166 FDA reports)
ARTHROPATHY ( 165 FDA reports)
MUCOSAL INFLAMMATION ( 165 FDA reports)
APHASIA ( 163 FDA reports)
FLUID RETENTION ( 163 FDA reports)
PRIMARY SEQUESTRUM ( 163 FDA reports)
EAR PAIN ( 161 FDA reports)
GRAND MAL CONVULSION ( 161 FDA reports)
PRODUCTIVE COUGH ( 161 FDA reports)
HEAD INJURY ( 160 FDA reports)
INTENTIONAL OVERDOSE ( 160 FDA reports)
SEPTIC SHOCK ( 160 FDA reports)
HAEMATURIA ( 159 FDA reports)
PARANOIA ( 158 FDA reports)
SKIN LESION ( 158 FDA reports)
BLINDNESS ( 157 FDA reports)
FEAR ( 156 FDA reports)
MOOD SWINGS ( 156 FDA reports)
RASH PRURITIC ( 156 FDA reports)
MOUTH ULCERATION ( 155 FDA reports)
HYPERSOMNIA ( 152 FDA reports)
LUNG DISORDER ( 152 FDA reports)
LUNG NEOPLASM ( 152 FDA reports)
RESTLESS LEGS SYNDROME ( 152 FDA reports)
RASH ERYTHEMATOUS ( 151 FDA reports)
RHEUMATOID ARTHRITIS ( 151 FDA reports)
ARRHYTHMIA ( 150 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 150 FDA reports)
DYSTONIA ( 149 FDA reports)
TOOTH ABSCESS ( 149 FDA reports)
SCOLIOSIS ( 148 FDA reports)
HEPATIC STEATOSIS ( 148 FDA reports)
CARDIOMYOPATHY ( 147 FDA reports)
NEUTROPHIL COUNT DECREASED ( 147 FDA reports)
RENAL DISORDER ( 147 FDA reports)
BLOOD SODIUM DECREASED ( 146 FDA reports)
LOOSE TOOTH ( 144 FDA reports)
OXYGEN SATURATION DECREASED ( 144 FDA reports)
TARDIVE DYSKINESIA ( 144 FDA reports)
TINNITUS ( 144 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 143 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 142 FDA reports)
PNEUMONIA ASPIRATION ( 142 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 141 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 141 FDA reports)
ARTERIOSCLEROSIS ( 140 FDA reports)
HEPATIC CYST ( 140 FDA reports)
MEDICATION ERROR ( 140 FDA reports)
CANDIDIASIS ( 139 FDA reports)
FACIAL PAIN ( 139 FDA reports)
EMOTIONAL DISORDER ( 138 FDA reports)
HYPERCHOLESTEROLAEMIA ( 138 FDA reports)
SPINAL COLUMN STENOSIS ( 138 FDA reports)
CRYING ( 137 FDA reports)
HEMIPARESIS ( 137 FDA reports)
NASAL CONGESTION ( 137 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 136 FDA reports)
BURSITIS ( 135 FDA reports)
ERECTILE DYSFUNCTION ( 135 FDA reports)
FOOT FRACTURE ( 135 FDA reports)
DISABILITY ( 134 FDA reports)
HALLUCINATION, VISUAL ( 134 FDA reports)
METASTASES TO LIVER ( 134 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 134 FDA reports)
SINUS TACHYCARDIA ( 134 FDA reports)
SINUS DISORDER ( 132 FDA reports)
SKIN EXFOLIATION ( 132 FDA reports)
GINGIVITIS ( 132 FDA reports)
MELAENA ( 132 FDA reports)
ENCEPHALOPATHY ( 131 FDA reports)
EPILEPSY ( 131 FDA reports)
ACCIDENTAL OVERDOSE ( 130 FDA reports)
INCONTINENCE ( 130 FDA reports)
FAECAL INCONTINENCE ( 129 FDA reports)
GALLBLADDER DISORDER ( 129 FDA reports)
PULMONARY HYPERTENSION ( 129 FDA reports)
ANOREXIA ( 128 FDA reports)
EMPHYSEMA ( 128 FDA reports)
SEROTONIN SYNDROME ( 127 FDA reports)
SKIN DISORDER ( 127 FDA reports)
DRY SKIN ( 126 FDA reports)
MENTAL IMPAIRMENT ( 126 FDA reports)
MOVEMENT DISORDER ( 125 FDA reports)
NIGHTMARE ( 125 FDA reports)
WALKING AID USER ( 125 FDA reports)
SPINAL COMPRESSION FRACTURE ( 124 FDA reports)
ABNORMAL DREAMS ( 123 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 123 FDA reports)
HEART RATE DECREASED ( 123 FDA reports)
LIFE EXPECTANCY SHORTENED ( 123 FDA reports)
LIMB INJURY ( 123 FDA reports)
IRRITABLE BOWEL SYNDROME ( 122 FDA reports)
PULMONARY CONGESTION ( 122 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 121 FDA reports)
INTERSTITIAL LUNG DISEASE ( 121 FDA reports)
SENSORY DISTURBANCE ( 121 FDA reports)
COMPRESSION FRACTURE ( 120 FDA reports)
HEPATITIS ( 120 FDA reports)
NIGHT SWEATS ( 120 FDA reports)
DIVERTICULITIS ( 119 FDA reports)
SKIN INDURATION ( 119 FDA reports)
ATAXIA ( 118 FDA reports)
BLOOD CALCIUM DECREASED ( 118 FDA reports)
FEELING COLD ( 118 FDA reports)
HEART RATE IRREGULAR ( 118 FDA reports)
MULTI-ORGAN FAILURE ( 118 FDA reports)
ABSCESS ( 117 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 117 FDA reports)
CARDIAC MURMUR ( 117 FDA reports)
COLONIC POLYP ( 117 FDA reports)
GINGIVAL BLEEDING ( 117 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 117 FDA reports)
LUMBAR SPINAL STENOSIS ( 117 FDA reports)
OESOPHAGITIS ( 117 FDA reports)
OSTEITIS ( 117 FDA reports)
DRUG INTOLERANCE ( 116 FDA reports)
HYPOTHYROIDISM ( 116 FDA reports)
PRESYNCOPE ( 116 FDA reports)
RASH GENERALISED ( 116 FDA reports)
PHYSICAL DISABILITY ( 115 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 113 FDA reports)
EATING DISORDER ( 113 FDA reports)
GASTRIC ULCER ( 113 FDA reports)
INFLAMMATION ( 113 FDA reports)
THINKING ABNORMAL ( 113 FDA reports)
VIRAL INFECTION ( 112 FDA reports)
ASCITES ( 112 FDA reports)
COLITIS ( 112 FDA reports)
FEMUR FRACTURE ( 112 FDA reports)
HEPATIC FAILURE ( 112 FDA reports)
MULTIPLE DRUG OVERDOSE ( 112 FDA reports)
BONE LOSS ( 111 FDA reports)
INTESTINAL OBSTRUCTION ( 111 FDA reports)
BLOOD POTASSIUM INCREASED ( 110 FDA reports)
HAEMODIALYSIS ( 110 FDA reports)
INJECTION SITE PRURITUS ( 110 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 109 FDA reports)
GASTROINTESTINAL DISORDER ( 109 FDA reports)
JOINT STIFFNESS ( 109 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 109 FDA reports)
SCIATICA ( 109 FDA reports)
TOOTH INFECTION ( 109 FDA reports)
CEREBRAL ATROPHY ( 108 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 108 FDA reports)
LEUKOCYTOSIS ( 108 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 108 FDA reports)
PHARYNGEAL OEDEMA ( 108 FDA reports)
ROTATOR CUFF SYNDROME ( 107 FDA reports)
SINUS BRADYCARDIA ( 107 FDA reports)
RHINORRHOEA ( 106 FDA reports)
ORTHOSTATIC HYPOTENSION ( 106 FDA reports)
PSORIASIS ( 106 FDA reports)
GLAUCOMA ( 105 FDA reports)
RESPIRATORY DISORDER ( 105 FDA reports)
FLUID OVERLOAD ( 104 FDA reports)
POISONING ( 104 FDA reports)
DEAFNESS ( 103 FDA reports)
DECUBITUS ULCER ( 103 FDA reports)
GINGIVAL DISORDER ( 103 FDA reports)
GOITRE ( 103 FDA reports)
ILL-DEFINED DISORDER ( 103 FDA reports)
PSYCHOTIC DISORDER ( 103 FDA reports)
TOOTH FRACTURE ( 103 FDA reports)
VENTRICULAR TACHYCARDIA ( 102 FDA reports)
DEBRIDEMENT ( 102 FDA reports)
GASTRIC DISORDER ( 102 FDA reports)
GOUT ( 102 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 101 FDA reports)
LIVER DISORDER ( 101 FDA reports)
RESPIRATORY DEPRESSION ( 101 FDA reports)
SWOLLEN TONGUE ( 101 FDA reports)
UPPER LIMB FRACTURE ( 101 FDA reports)
BACK DISORDER ( 100 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 100 FDA reports)
INJECTION SITE REACTION ( 100 FDA reports)
METABOLIC ACIDOSIS ( 100 FDA reports)
OSTEOLYSIS ( 100 FDA reports)
PANCREATITIS ACUTE ( 100 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 100 FDA reports)
POOR QUALITY SLEEP ( 100 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 99 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 99 FDA reports)
FISTULA ( 99 FDA reports)
SPONDYLOLISTHESIS ( 99 FDA reports)
RADICULOPATHY ( 98 FDA reports)
ORAL CANDIDIASIS ( 98 FDA reports)
ANKLE FRACTURE ( 96 FDA reports)
BIPOLAR DISORDER ( 96 FDA reports)
BLOOD ALBUMIN DECREASED ( 96 FDA reports)
DELUSION ( 96 FDA reports)
DIALYSIS ( 96 FDA reports)
DRUG LEVEL INCREASED ( 95 FDA reports)
HAEMATOMA ( 95 FDA reports)
MASS ( 95 FDA reports)
MICTURITION URGENCY ( 95 FDA reports)
MULTIPLE INJURIES ( 95 FDA reports)
MUSCLE TIGHTNESS ( 95 FDA reports)
SPINAL FRACTURE ( 95 FDA reports)
SENSORY LOSS ( 94 FDA reports)
HYPOMAGNESAEMIA ( 94 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 94 FDA reports)
MYOPATHY ( 94 FDA reports)
PULMONARY FIBROSIS ( 94 FDA reports)
BONE DENSITY DECREASED ( 93 FDA reports)
GENERALISED OEDEMA ( 93 FDA reports)
HYPERCALCAEMIA ( 93 FDA reports)
INJECTION SITE SWELLING ( 93 FDA reports)
MYELODYSPLASTIC SYNDROME ( 93 FDA reports)
NO THERAPEUTIC RESPONSE ( 93 FDA reports)
PERICARDIAL EFFUSION ( 93 FDA reports)
SKIN HYPERTROPHY ( 93 FDA reports)
EYE DISORDER ( 92 FDA reports)
METASTASES TO LUNG ( 92 FDA reports)
MOOD ALTERED ( 92 FDA reports)
ADVERSE DRUG REACTION ( 91 FDA reports)
ADVERSE EVENT ( 91 FDA reports)
BASAL CELL CARCINOMA ( 91 FDA reports)
BEDRIDDEN ( 91 FDA reports)
CEREBRAL INFARCTION ( 91 FDA reports)
MYOCARDIAL ISCHAEMIA ( 91 FDA reports)
SPINAL DISORDER ( 91 FDA reports)
STATUS EPILEPTICUS ( 91 FDA reports)
EJECTION FRACTION DECREASED ( 90 FDA reports)
HAEMOPTYSIS ( 89 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 89 FDA reports)
HYPOKINESIA ( 88 FDA reports)
LOWER LIMB FRACTURE ( 88 FDA reports)
MENISCUS LESION ( 88 FDA reports)
PROSTATE CANCER ( 88 FDA reports)
SKIN BURNING SENSATION ( 88 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 87 FDA reports)
COAGULOPATHY ( 87 FDA reports)
PARALYSIS ( 87 FDA reports)
POST PROCEDURAL COMPLICATION ( 87 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 86 FDA reports)
SQUAMOUS CELL CARCINOMA ( 85 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 85 FDA reports)
BREAST CANCER ( 85 FDA reports)
INJECTION SITE HAEMORRHAGE ( 85 FDA reports)
ECZEMA ( 84 FDA reports)
JOINT DISLOCATION ( 84 FDA reports)
MAJOR DEPRESSION ( 84 FDA reports)
PYELONEPHRITIS ( 84 FDA reports)
TENDONITIS ( 83 FDA reports)
DEVICE RELATED INFECTION ( 83 FDA reports)
GASTROENTERITIS ( 83 FDA reports)
HYPERAESTHESIA ( 83 FDA reports)
MASTICATION DISORDER ( 83 FDA reports)
ONYCHOMYCOSIS ( 83 FDA reports)
HOSPITALISATION ( 82 FDA reports)
LACTIC ACIDOSIS ( 82 FDA reports)
SKIN TIGHTNESS ( 82 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 82 FDA reports)
SOMNAMBULISM ( 81 FDA reports)
CHOLECYSTITIS CHRONIC ( 81 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 81 FDA reports)
DRUG ADMINISTRATION ERROR ( 81 FDA reports)
FLANK PAIN ( 81 FDA reports)
HYPOAESTHESIA ORAL ( 81 FDA reports)
HYPOCALCAEMIA ( 81 FDA reports)
LIMB DISCOMFORT ( 81 FDA reports)
LYMPHOEDEMA ( 81 FDA reports)
BONE MARROW FAILURE ( 80 FDA reports)
DIABETIC KETOACIDOSIS ( 80 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 80 FDA reports)
HYPERKERATOSIS ( 80 FDA reports)
ILEUS ( 80 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 80 FDA reports)
BLOOD BILIRUBIN INCREASED ( 79 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 79 FDA reports)
NEURITIS ( 79 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 79 FDA reports)
VITREOUS FLOATERS ( 79 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 78 FDA reports)
BLADDER DISORDER ( 78 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 78 FDA reports)
HEMIPLEGIA ( 78 FDA reports)
ABDOMINAL PAIN LOWER ( 77 FDA reports)
AORTIC ANEURYSM ( 77 FDA reports)
CAROTID ARTERY STENOSIS ( 77 FDA reports)
EXPOSED BONE IN JAW ( 77 FDA reports)
GINGIVAL PAIN ( 77 FDA reports)
JOINT INJURY ( 77 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 77 FDA reports)
SYNOVIAL CYST ( 77 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 76 FDA reports)
THYROID NEOPLASM ( 76 FDA reports)
AREFLEXIA ( 76 FDA reports)
EXCORIATION ( 76 FDA reports)
LIBIDO DECREASED ( 76 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 76 FDA reports)
MYOTONIA ( 76 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 75 FDA reports)
BODY HEIGHT DECREASED ( 75 FDA reports)
GROIN PAIN ( 75 FDA reports)
HEPATIC LESION ( 75 FDA reports)
JOINT EFFUSION ( 75 FDA reports)
NERVE INJURY ( 75 FDA reports)
CROHN'S DISEASE ( 74 FDA reports)
DRUG SCREEN POSITIVE ( 74 FDA reports)
FACIAL BONES FRACTURE ( 74 FDA reports)
HYPOPHOSPHATAEMIA ( 74 FDA reports)
LUNG NEOPLASM MALIGNANT ( 74 FDA reports)
PHARYNGITIS ( 74 FDA reports)
NODULE ( 73 FDA reports)
OTITIS MEDIA ( 73 FDA reports)
SENSATION OF HEAVINESS ( 73 FDA reports)
STEVENS-JOHNSON SYNDROME ( 72 FDA reports)
CEREBRAL HAEMORRHAGE ( 72 FDA reports)
FIBROSIS ( 72 FDA reports)
HEARING IMPAIRED ( 72 FDA reports)
HERNIA ( 72 FDA reports)
LIP SWELLING ( 72 FDA reports)
NEOPLASM PROGRESSION ( 72 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 71 FDA reports)
CHOLECYSTITIS ( 71 FDA reports)
TONGUE ULCERATION ( 71 FDA reports)
TRIGEMINAL NEURALGIA ( 71 FDA reports)
HYPERTONIC BLADDER ( 70 FDA reports)
PETECHIAE ( 70 FDA reports)
GINGIVAL SWELLING ( 69 FDA reports)
GLOSSODYNIA ( 69 FDA reports)
JAW DISORDER ( 69 FDA reports)
PALLOR ( 69 FDA reports)
PERIODONTAL DISEASE ( 69 FDA reports)
TRISMUS ( 69 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 68 FDA reports)
CHROMATURIA ( 68 FDA reports)
DRUG DISPENSING ERROR ( 68 FDA reports)
EAR INFECTION ( 68 FDA reports)
ESCHERICHIA INFECTION ( 68 FDA reports)
JAW FRACTURE ( 68 FDA reports)
KIDNEY INFECTION ( 68 FDA reports)
LEFT ATRIAL DILATATION ( 68 FDA reports)
METASTASES TO SPINE ( 68 FDA reports)
OPTIC NEURITIS ( 68 FDA reports)
PRURITUS GENERALISED ( 68 FDA reports)
LOCALISED INFECTION ( 67 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 67 FDA reports)
NEUROGENIC BLADDER ( 67 FDA reports)
PROTHROMBIN TIME PROLONGED ( 67 FDA reports)
RESPIRATORY TRACT INFECTION ( 67 FDA reports)
STEM CELL TRANSPLANT ( 66 FDA reports)
THROAT IRRITATION ( 66 FDA reports)
WOUND ( 66 FDA reports)
ACIDOSIS ( 66 FDA reports)
ACTINOMYCOSIS ( 66 FDA reports)
HALLUCINATION, AUDITORY ( 66 FDA reports)
HYDRONEPHROSIS ( 66 FDA reports)
LOCAL SWELLING ( 66 FDA reports)
MUSCLE STRAIN ( 66 FDA reports)
PERONEAL NERVE PALSY ( 66 FDA reports)
PNEUMONITIS ( 66 FDA reports)
PROTEINURIA ( 66 FDA reports)
ANORGASMIA ( 65 FDA reports)
CEREBRAL ISCHAEMIA ( 65 FDA reports)
DIVERTICULUM INTESTINAL ( 65 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 65 FDA reports)
INADEQUATE ANALGESIA ( 65 FDA reports)
JAUNDICE ( 65 FDA reports)
MALIGNANT MELANOMA ( 65 FDA reports)
MYOSITIS ( 65 FDA reports)
PHOTOPHOBIA ( 65 FDA reports)
THROAT TIGHTNESS ( 65 FDA reports)
UROSEPSIS ( 65 FDA reports)
TENDERNESS ( 64 FDA reports)
ULCER ( 64 FDA reports)
URINE OUTPUT DECREASED ( 64 FDA reports)
ACUTE RESPIRATORY FAILURE ( 64 FDA reports)
ANGINA UNSTABLE ( 64 FDA reports)
BLOOD IRON DECREASED ( 64 FDA reports)
BREAST CANCER RECURRENT ( 64 FDA reports)
CHOLECYSTECTOMY ( 64 FDA reports)
COLD SWEAT ( 64 FDA reports)
EYE SWELLING ( 64 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 64 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 64 FDA reports)
INFUSION RELATED REACTION ( 64 FDA reports)
LACERATION ( 64 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 64 FDA reports)
ANAPHYLACTIC REACTION ( 63 FDA reports)
CHRONIC SINUSITIS ( 63 FDA reports)
FEELING JITTERY ( 63 FDA reports)
GASTROENTERITIS VIRAL ( 63 FDA reports)
HYPOACUSIS ( 63 FDA reports)
IMPAIRED DRIVING ABILITY ( 63 FDA reports)
IMPAIRED WORK ABILITY ( 63 FDA reports)
MANIA ( 63 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 63 FDA reports)
OCULAR HYPERAEMIA ( 63 FDA reports)
PERIPHERAL COLDNESS ( 63 FDA reports)
PURULENCE ( 63 FDA reports)
RENAL TUBULAR NECROSIS ( 63 FDA reports)
QUALITY OF LIFE DECREASED ( 62 FDA reports)
RHINITIS ALLERGIC ( 62 FDA reports)
SHOCK ( 62 FDA reports)
SKIN LACERATION ( 62 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 62 FDA reports)
EUPHORIC MOOD ( 62 FDA reports)
HAND FRACTURE ( 62 FDA reports)
LUMBAR RADICULOPATHY ( 62 FDA reports)
NO ADVERSE EVENT ( 62 FDA reports)
ODYNOPHAGIA ( 62 FDA reports)
BLOOD URINE PRESENT ( 61 FDA reports)
DENTURE WEARER ( 61 FDA reports)
DRUG ABUSER ( 61 FDA reports)
PLEURITIC PAIN ( 61 FDA reports)
RASH MACULAR ( 61 FDA reports)
RETCHING ( 61 FDA reports)
THIRST ( 61 FDA reports)
VENTRICULAR FIBRILLATION ( 61 FDA reports)
ACTINIC KERATOSIS ( 60 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 60 FDA reports)
BLINDNESS UNILATERAL ( 60 FDA reports)
CORONARY ARTERY OCCLUSION ( 60 FDA reports)
DEMENTIA ( 60 FDA reports)
DYSPHEMIA ( 60 FDA reports)
PATHOLOGICAL FRACTURE ( 60 FDA reports)
ABDOMINAL TENDERNESS ( 59 FDA reports)
ASPIRATION ( 59 FDA reports)
BACK INJURY ( 59 FDA reports)
BODY TEMPERATURE INCREASED ( 59 FDA reports)
DRUG ERUPTION ( 59 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 59 FDA reports)
RASH PAPULAR ( 59 FDA reports)
VISUAL DISTURBANCE ( 59 FDA reports)
SINUS HEADACHE ( 58 FDA reports)
TRANSAMINASES INCREASED ( 58 FDA reports)
TYPE 1 DIABETES MELLITUS ( 58 FDA reports)
VASCULITIS ( 58 FDA reports)
VISUAL FIELD DEFECT ( 58 FDA reports)
WOUND DEHISCENCE ( 58 FDA reports)
CATARACT OPERATION ( 58 FDA reports)
FACET JOINT SYNDROME ( 58 FDA reports)
INCOHERENT ( 58 FDA reports)
NERVE COMPRESSION ( 58 FDA reports)
NEUROPATHY ( 58 FDA reports)
ABSCESS DRAINAGE ( 57 FDA reports)
APATHY ( 57 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 57 FDA reports)
FAECES DISCOLOURED ( 57 FDA reports)
LACRIMATION INCREASED ( 57 FDA reports)
LOBAR PNEUMONIA ( 57 FDA reports)
MOTOR DYSFUNCTION ( 57 FDA reports)
ORAL SURGERY ( 57 FDA reports)
POLYNEUROPATHY ( 57 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 56 FDA reports)
DERMATITIS CONTACT ( 56 FDA reports)
DRUG PRESCRIBING ERROR ( 56 FDA reports)
ELECTROLYTE IMBALANCE ( 56 FDA reports)
HEPATITIS C ( 56 FDA reports)
INGROWING NAIL ( 56 FDA reports)
KNEE ARTHROPLASTY ( 56 FDA reports)
LUNG INFECTION ( 56 FDA reports)
PURULENT DISCHARGE ( 56 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 56 FDA reports)
THYROID DISORDER ( 56 FDA reports)
FAILURE TO THRIVE ( 55 FDA reports)
NEUROTOXICITY ( 55 FDA reports)
PLEURAL FIBROSIS ( 55 FDA reports)
POLYURIA ( 55 FDA reports)
ACUTE CORONARY SYNDROME ( 54 FDA reports)
BLINDNESS TRANSIENT ( 54 FDA reports)
CIRCULATORY COLLAPSE ( 54 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 54 FDA reports)
CYANOSIS ( 54 FDA reports)
DYSAESTHESIA ( 54 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 54 FDA reports)
HYPOAESTHESIA FACIAL ( 54 FDA reports)
BACTERAEMIA ( 53 FDA reports)
BREATH ODOUR ( 53 FDA reports)
DEAFNESS NEUROSENSORY ( 53 FDA reports)
DERMAL CYST ( 53 FDA reports)
HAEMOLYTIC ANAEMIA ( 53 FDA reports)
HYPOVOLAEMIA ( 53 FDA reports)
NOCTURIA ( 53 FDA reports)
OSTEOSCLEROSIS ( 53 FDA reports)
PERITONITIS ( 53 FDA reports)
PNEUMOTHORAX ( 53 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 53 FDA reports)
SKIN CANCER ( 53 FDA reports)
RENAL PAIN ( 52 FDA reports)
SKIN FIBROSIS ( 52 FDA reports)
SKIN HYPERPIGMENTATION ( 52 FDA reports)
WHEELCHAIR USER ( 52 FDA reports)
AZOTAEMIA ( 52 FDA reports)
CERVICAL SPINAL STENOSIS ( 52 FDA reports)
CHOKING ( 52 FDA reports)
GANGRENE ( 52 FDA reports)
JAW OPERATION ( 52 FDA reports)
MUSCLE ATROPHY ( 52 FDA reports)
MUSCLE DISORDER ( 52 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 52 FDA reports)
AGRANULOCYTOSIS ( 51 FDA reports)
CARDIOVASCULAR DISORDER ( 51 FDA reports)
DEPENDENCE ( 51 FDA reports)
DIABETIC RETINOPATHY ( 51 FDA reports)
HUMERUS FRACTURE ( 51 FDA reports)
INCREASED TENDENCY TO BRUISE ( 51 FDA reports)
ORAL HERPES ( 51 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 51 FDA reports)
PLASMACYTOMA ( 51 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 51 FDA reports)
STOMACH DISCOMFORT ( 51 FDA reports)
SUBDURAL HAEMATOMA ( 50 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 50 FDA reports)
VIITH NERVE PARALYSIS ( 50 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 50 FDA reports)
CLUMSINESS ( 50 FDA reports)
FACE OEDEMA ( 50 FDA reports)
FEELING DRUNK ( 50 FDA reports)
GINGIVAL INFECTION ( 50 FDA reports)
JOINT CONTRACTURE ( 50 FDA reports)
LIVER INJURY ( 50 FDA reports)
ACCIDENTAL EXPOSURE ( 49 FDA reports)
ANGIOEDEMA ( 49 FDA reports)
LARYNGITIS ( 49 FDA reports)
MIDDLE INSOMNIA ( 49 FDA reports)
OPEN WOUND ( 49 FDA reports)
PROCEDURAL PAIN ( 49 FDA reports)
RHINITIS ( 49 FDA reports)
SEQUESTRECTOMY ( 48 FDA reports)
ABSCESS JAW ( 48 FDA reports)
AORTIC VALVE INCOMPETENCE ( 48 FDA reports)
BLOOD MAGNESIUM DECREASED ( 48 FDA reports)
BONE DEBRIDEMENT ( 48 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 48 FDA reports)
FRACTURE ( 48 FDA reports)
HEPATIC CIRRHOSIS ( 48 FDA reports)
HYPOVENTILATION ( 48 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 48 FDA reports)
IRON DEFICIENCY ANAEMIA ( 48 FDA reports)
NEUTROPENIC SEPSIS ( 48 FDA reports)
PARKINSON'S DISEASE ( 48 FDA reports)
PARKINSONISM ( 48 FDA reports)
POST HERPETIC NEURALGIA ( 48 FDA reports)
ACUTE SINUSITIS ( 47 FDA reports)
ADRENAL INSUFFICIENCY ( 47 FDA reports)
BLOOD CALCIUM INCREASED ( 47 FDA reports)
CORONARY ARTERY BYPASS ( 47 FDA reports)
DIFFICULTY IN WALKING ( 47 FDA reports)
DISEASE RECURRENCE ( 47 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 47 FDA reports)
PAIN OF SKIN ( 47 FDA reports)
PARAPLEGIA ( 47 FDA reports)
PHOTOPSIA ( 47 FDA reports)
PRESBYOPIA ( 47 FDA reports)
SEASONAL ALLERGY ( 47 FDA reports)
SEBORRHOEIC KERATOSIS ( 47 FDA reports)
SERUM FERRITIN INCREASED ( 47 FDA reports)
SLEEP TALKING ( 47 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 47 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 47 FDA reports)
RESPIRATORY RATE INCREASED ( 46 FDA reports)
WRIST FRACTURE ( 46 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 46 FDA reports)
CYST ( 46 FDA reports)
DEVICE MALFUNCTION ( 46 FDA reports)
EYE INFECTION ( 46 FDA reports)
LIGAMENT SPRAIN ( 46 FDA reports)
MACULAR DEGENERATION ( 46 FDA reports)
MEDICATION RESIDUE ( 46 FDA reports)
MITRAL VALVE PROLAPSE ( 46 FDA reports)
MUSCLE RIGIDITY ( 46 FDA reports)
ORAL INFECTION ( 46 FDA reports)
ORAL INTAKE REDUCED ( 46 FDA reports)
AFFECTIVE DISORDER ( 45 FDA reports)
AKATHISIA ( 45 FDA reports)
AUTOIMMUNE HEPATITIS ( 45 FDA reports)
BRUXISM ( 45 FDA reports)
CAROTID BRUIT ( 45 FDA reports)
CLOSTRIDIAL INFECTION ( 45 FDA reports)
EYE IRRITATION ( 45 FDA reports)
EYELID OEDEMA ( 45 FDA reports)
FACIAL PALSY ( 45 FDA reports)
HERPES SIMPLEX ( 45 FDA reports)
HYPERTHERMIA ( 45 FDA reports)
HYPOTONIA ( 45 FDA reports)
INTESTINAL PERFORATION ( 45 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 45 FDA reports)
MONOCYTE COUNT INCREASED ( 45 FDA reports)
NARCOLEPSY ( 45 FDA reports)
PLANTAR FASCIITIS ( 45 FDA reports)
PROCTALGIA ( 45 FDA reports)
RADIOTHERAPY ( 45 FDA reports)
TEMPERATURE INTOLERANCE ( 45 FDA reports)
UTERINE LEIOMYOMA ( 45 FDA reports)
RENAL INJURY ( 44 FDA reports)
RESORPTION BONE INCREASED ( 44 FDA reports)
VAGINAL HAEMORRHAGE ( 44 FDA reports)
BACTERIAL INFECTION ( 44 FDA reports)
BONE OPERATION ( 44 FDA reports)
COLITIS ISCHAEMIC ( 44 FDA reports)
EYE MOVEMENT DISORDER ( 44 FDA reports)
FOOT DEFORMITY ( 44 FDA reports)
GRANULOCYTOPENIA ( 44 FDA reports)
HIP ARTHROPLASTY ( 44 FDA reports)
HOMICIDAL IDEATION ( 44 FDA reports)
LUNG CONSOLIDATION ( 44 FDA reports)
MALNUTRITION ( 44 FDA reports)
MENINGITIS ( 44 FDA reports)
MUCOUS MEMBRANE DISORDER ( 44 FDA reports)
NASAL SEPTUM DEVIATION ( 44 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 44 FDA reports)
OEDEMA MOUTH ( 44 FDA reports)
PATHOLOGICAL GAMBLING ( 44 FDA reports)
PLASMACYTOSIS ( 44 FDA reports)
ACNE ( 43 FDA reports)
DECREASED ACTIVITY ( 43 FDA reports)
EYE HAEMORRHAGE ( 43 FDA reports)
LEG AMPUTATION ( 43 FDA reports)
PARAESTHESIA ORAL ( 43 FDA reports)
PERIODONTITIS ( 43 FDA reports)
PREGNANCY ( 43 FDA reports)
ACCIDENT ( 42 FDA reports)
AGEUSIA ( 42 FDA reports)
CARDIOGENIC SHOCK ( 42 FDA reports)
CAROTID ARTERY DISEASE ( 42 FDA reports)
DERMATITIS ( 42 FDA reports)
DIABETIC COMA ( 42 FDA reports)
FUNGAL INFECTION ( 42 FDA reports)
GASTRIC HAEMORRHAGE ( 42 FDA reports)
GLOSSITIS ( 42 FDA reports)
HYSTERECTOMY ( 42 FDA reports)
KYPHOSIS ( 42 FDA reports)
LYMPHOMA ( 42 FDA reports)
MENORRHAGIA ( 42 FDA reports)
PELVIC FRACTURE ( 42 FDA reports)
SCHIZOPHRENIA ( 42 FDA reports)
TONGUE INJURY ( 42 FDA reports)
TORSADE DE POINTES ( 42 FDA reports)
TUMOUR LYSIS SYNDROME ( 42 FDA reports)
VENOUS THROMBOSIS ( 42 FDA reports)
SINUS CONGESTION ( 41 FDA reports)
SPLENOMEGALY ( 41 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 41 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 41 FDA reports)
URINARY HESITATION ( 41 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 41 FDA reports)
ABORTION SPONTANEOUS ( 41 FDA reports)
BLOOD PRESSURE ABNORMAL ( 41 FDA reports)
ESSENTIAL HYPERTENSION ( 41 FDA reports)
FACE INJURY ( 41 FDA reports)
HEPATOMEGALY ( 41 FDA reports)
HOSTILITY ( 41 FDA reports)
ONYCHOCLASIS ( 41 FDA reports)
PELVIC PAIN ( 41 FDA reports)
BREAST PAIN ( 40 FDA reports)
COLLAPSE OF LUNG ( 40 FDA reports)
CONCUSSION ( 40 FDA reports)
DEVICE FAILURE ( 40 FDA reports)
ECCHYMOSIS ( 40 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 40 FDA reports)
ENDODONTIC PROCEDURE ( 40 FDA reports)
EYE PRURITUS ( 40 FDA reports)
GINGIVAL RECESSION ( 40 FDA reports)
HYPERPHAGIA ( 40 FDA reports)
INJECTION SITE IRRITATION ( 40 FDA reports)
INJECTION SITE WARMTH ( 40 FDA reports)
ONYCHALGIA ( 40 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 40 FDA reports)
WOUND DRAINAGE ( 40 FDA reports)
RALES ( 39 FDA reports)
SPUTUM DISCOLOURED ( 39 FDA reports)
VITAMIN D DEFICIENCY ( 39 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 39 FDA reports)
ABDOMINAL MASS ( 39 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 39 FDA reports)
DEMYELINATION ( 39 FDA reports)
DENTAL FISTULA ( 39 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 39 FDA reports)
FAECALOMA ( 39 FDA reports)
GRIP STRENGTH DECREASED ( 39 FDA reports)
HEPATIC NECROSIS ( 39 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 39 FDA reports)
MEDICAL DEVICE COMPLICATION ( 39 FDA reports)
NAIL DISORDER ( 39 FDA reports)
PHLEBITIS ( 39 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 39 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 39 FDA reports)
ATRIOVENTRICULAR BLOCK ( 38 FDA reports)
BLOOD CHLORIDE DECREASED ( 38 FDA reports)
BRONCHOPNEUMONIA ( 38 FDA reports)
ENTEROCOCCAL INFECTION ( 38 FDA reports)
GASTROINTESTINAL PAIN ( 38 FDA reports)
GYNAECOMASTIA ( 38 FDA reports)
HUNGER ( 38 FDA reports)
INGUINAL HERNIA ( 38 FDA reports)
INJECTION SITE RASH ( 38 FDA reports)
ISCHAEMIA ( 38 FDA reports)
LYMPHOPENIA ( 38 FDA reports)
MELANOCYTIC NAEVUS ( 38 FDA reports)
METABOLIC ENCEPHALOPATHY ( 38 FDA reports)
METASTATIC NEOPLASM ( 38 FDA reports)
RECTOCELE ( 38 FDA reports)
SEROMA ( 38 FDA reports)
SPINAL LAMINECTOMY ( 38 FDA reports)
TACHYPNOEA ( 38 FDA reports)
VARICOSE VEIN ( 38 FDA reports)
SCAB ( 37 FDA reports)
SCREAMING ( 37 FDA reports)
SINUS ARRHYTHMIA ( 37 FDA reports)
SKIN ATROPHY ( 37 FDA reports)
SOFT TISSUE DISORDER ( 37 FDA reports)
SPINAL COLUMN INJURY ( 37 FDA reports)
SPINAL CORD COMPRESSION ( 37 FDA reports)
TENDON DISORDER ( 37 FDA reports)
VAGINAL INFECTION ( 37 FDA reports)
ANOXIC ENCEPHALOPATHY ( 37 FDA reports)
APNOEA ( 37 FDA reports)
BLADDER SPASM ( 37 FDA reports)
CARDIAC ENZYMES INCREASED ( 37 FDA reports)
CERUMEN IMPACTION ( 37 FDA reports)
COMPLEX PARTIAL SEIZURES ( 37 FDA reports)
ERUCTATION ( 37 FDA reports)
HEART VALVE INCOMPETENCE ( 37 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 37 FDA reports)
INJECTION SITE MASS ( 37 FDA reports)
MUSCULOSKELETAL DISORDER ( 37 FDA reports)
NECROSIS ( 37 FDA reports)
ORAL CAVITY FISTULA ( 37 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 37 FDA reports)
PULMONARY MASS ( 37 FDA reports)
ABDOMINAL HERNIA ( 36 FDA reports)
ANEURYSM ( 36 FDA reports)
APHAGIA ( 36 FDA reports)
APPLICATION SITE ERYTHEMA ( 36 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 36 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 36 FDA reports)
BRAIN OEDEMA ( 36 FDA reports)
CORONARY ARTERY STENOSIS ( 36 FDA reports)
DERMATITIS EXFOLIATIVE ( 36 FDA reports)
DIABETIC FOOT ( 36 FDA reports)
EOSINOPHIL COUNT INCREASED ( 36 FDA reports)
HYPERTENSIVE CRISIS ( 36 FDA reports)
LARGE INTESTINE PERFORATION ( 36 FDA reports)
MACULOPATHY ( 36 FDA reports)
MUSCLE CONTRACTURE ( 36 FDA reports)
PANIC REACTION ( 36 FDA reports)
PARTIAL SEIZURES ( 36 FDA reports)
PROTEIN TOTAL DECREASED ( 36 FDA reports)
RESPIRATORY RATE DECREASED ( 36 FDA reports)
WEIGHT FLUCTUATION ( 36 FDA reports)
SENSITIVITY OF TEETH ( 35 FDA reports)
SUDDEN DEATH ( 35 FDA reports)
WOUND INFECTION ( 35 FDA reports)
AFFECT LABILITY ( 35 FDA reports)
BRAIN INJURY ( 35 FDA reports)
CERVICAL DYSPLASIA ( 35 FDA reports)
CHOLESTASIS ( 35 FDA reports)
CYSTOCELE ( 35 FDA reports)
GENITAL HERPES ( 35 FDA reports)
HEPATIC ENCEPHALOPATHY ( 35 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 35 FDA reports)
POOR PERIPHERAL CIRCULATION ( 35 FDA reports)
POSTURE ABNORMAL ( 35 FDA reports)
ATRIAL FLUTTER ( 34 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 34 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 34 FDA reports)
BLOOD DISORDER ( 34 FDA reports)
BRONCHIECTASIS ( 34 FDA reports)
CHONDROMALACIA ( 34 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 34 FDA reports)
EYELID PTOSIS ( 34 FDA reports)
GENERALISED ERYTHEMA ( 34 FDA reports)
GINGIVAL ULCERATION ( 34 FDA reports)
INTENTIONAL MISUSE ( 34 FDA reports)
LEUKOENCEPHALOPATHY ( 34 FDA reports)
NYSTAGMUS ( 34 FDA reports)
PHOTOSENSITIVITY REACTION ( 34 FDA reports)
RESPIRATORY TRACT CONGESTION ( 34 FDA reports)
RHONCHI ( 34 FDA reports)
SEXUAL DYSFUNCTION ( 34 FDA reports)
SNORING ( 34 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 34 FDA reports)
TONGUE DISCOLOURATION ( 34 FDA reports)
VASODILATATION ( 34 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 34 FDA reports)
VERTEBROPLASTY ( 34 FDA reports)
RASH MACULO-PAPULAR ( 33 FDA reports)
RESPIRATORY ACIDOSIS ( 33 FDA reports)
SALIVARY HYPERSECRETION ( 33 FDA reports)
VAGINAL DISCHARGE ( 33 FDA reports)
VENTRICULAR HYPERTROPHY ( 33 FDA reports)
WRONG DRUG ADMINISTERED ( 33 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 33 FDA reports)
ANAL SPHINCTER ATONY ( 33 FDA reports)
APPENDICITIS ( 33 FDA reports)
ASTERIXIS ( 33 FDA reports)
BODY TEMPERATURE DECREASED ( 33 FDA reports)
BREAST MASS ( 33 FDA reports)
CATHETER PLACEMENT ( 33 FDA reports)
DILATATION VENTRICULAR ( 33 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 33 FDA reports)
EAR CONGESTION ( 33 FDA reports)
HEPATIC MASS ( 33 FDA reports)
HEPATOTOXICITY ( 33 FDA reports)
MYDRIASIS ( 33 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 33 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 33 FDA reports)
BARRETT'S OESOPHAGUS ( 32 FDA reports)
BONE EROSION ( 32 FDA reports)
CAESAREAN SECTION ( 32 FDA reports)
CARDIAC VALVE DISEASE ( 32 FDA reports)
CULTURE URINE POSITIVE ( 32 FDA reports)
DENTAL CARE ( 32 FDA reports)
DIABETIC NEPHROPATHY ( 32 FDA reports)
DRUG LEVEL DECREASED ( 32 FDA reports)
HAEMARTHROSIS ( 32 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 32 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 32 FDA reports)
MUCOSAL ULCERATION ( 32 FDA reports)
NECK INJURY ( 32 FDA reports)
OESOPHAGEAL DISORDER ( 32 FDA reports)
ORAL DISCOMFORT ( 32 FDA reports)
PETIT MAL EPILEPSY ( 32 FDA reports)
PIGMENTATION DISORDER ( 32 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 32 FDA reports)
PRODUCT ADHESION ISSUE ( 32 FDA reports)
PULSE ABSENT ( 32 FDA reports)
TROPONIN INCREASED ( 32 FDA reports)
WALKING DISABILITY ( 32 FDA reports)
RETINAL HAEMORRHAGE ( 31 FDA reports)
SENSATION OF FOREIGN BODY ( 31 FDA reports)
SPINAL DECOMPRESSION ( 31 FDA reports)
SUBCUTANEOUS ABSCESS ( 31 FDA reports)
ANAEMIA POSTOPERATIVE ( 31 FDA reports)
ANGIOPATHY ( 31 FDA reports)
BLADDER OPERATION ( 31 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 31 FDA reports)
BODY DYSMORPHIC DISORDER ( 31 FDA reports)
BREAST CANCER METASTATIC ( 31 FDA reports)
DILATATION ATRIAL ( 31 FDA reports)
DYSLIPIDAEMIA ( 31 FDA reports)
ENCEPHALITIS ( 31 FDA reports)
FORMICATION ( 31 FDA reports)
IMMUNE SYSTEM DISORDER ( 31 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 31 FDA reports)
LABORATORY TEST ABNORMAL ( 31 FDA reports)
MUSCLE SPASTICITY ( 31 FDA reports)
PERIPHERAL ISCHAEMIA ( 31 FDA reports)
PLATELET COUNT INCREASED ( 31 FDA reports)
ACUTE HEPATIC FAILURE ( 30 FDA reports)
AORTIC CALCIFICATION ( 30 FDA reports)
APHONIA ( 30 FDA reports)
APPLICATION SITE RASH ( 30 FDA reports)
ARTHROPOD BITE ( 30 FDA reports)
BONE NEOPLASM MALIGNANT ( 30 FDA reports)
BRAIN NEOPLASM ( 30 FDA reports)
BRONCHITIS CHRONIC ( 30 FDA reports)
EXPIRED DRUG ADMINISTERED ( 30 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 30 FDA reports)
GASTRIC POLYPS ( 30 FDA reports)
GASTRITIS EROSIVE ( 30 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 30 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 30 FDA reports)
LIPOMA ( 30 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 30 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 30 FDA reports)
RADIUS FRACTURE ( 30 FDA reports)
SKIN SWELLING ( 30 FDA reports)
PURPURA ( 29 FDA reports)
SCRATCH ( 29 FDA reports)
ATONIC URINARY BLADDER ( 29 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 29 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 29 FDA reports)
COLON CANCER ( 29 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 29 FDA reports)
CONJUNCTIVITIS ( 29 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 29 FDA reports)
DYSGRAPHIA ( 29 FDA reports)
FOREIGN BODY ( 29 FDA reports)
HYPERTENSIVE HEART DISEASE ( 29 FDA reports)
LACUNAR INFARCTION ( 29 FDA reports)
LOSS OF CONTROL OF LEGS ( 29 FDA reports)
MYELITIS TRANSVERSE ( 29 FDA reports)
ANURIA ( 28 FDA reports)
APLASTIC ANAEMIA ( 28 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 28 FDA reports)
BLOOD BICARBONATE DECREASED ( 28 FDA reports)
CHEST X-RAY ABNORMAL ( 28 FDA reports)
CHOREA ( 28 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 28 FDA reports)
EROSIVE OESOPHAGITIS ( 28 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 28 FDA reports)
HAEMANGIOMA ( 28 FDA reports)
HILAR LYMPHADENOPATHY ( 28 FDA reports)
HYPERNATRAEMIA ( 28 FDA reports)
HYPERPARATHYROIDISM ( 28 FDA reports)
HYPERREFLEXIA ( 28 FDA reports)
JUGULAR VEIN THROMBOSIS ( 28 FDA reports)
MIOSIS ( 28 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 28 FDA reports)
PARAPROTEINAEMIA ( 28 FDA reports)
PLEURISY ( 28 FDA reports)
PROCEDURAL COMPLICATION ( 28 FDA reports)
PSYCHIATRIC SYMPTOM ( 28 FDA reports)
PYURIA ( 28 FDA reports)
SICK SINUS SYNDROME ( 28 FDA reports)
SKELETAL INJURY ( 28 FDA reports)
SLUGGISHNESS ( 28 FDA reports)
STENT PLACEMENT ( 28 FDA reports)
THERAPY NON-RESPONDER ( 28 FDA reports)
TONGUE DISORDER ( 28 FDA reports)
URINE ODOUR ABNORMAL ( 28 FDA reports)
UTERINE POLYP ( 28 FDA reports)
RECTAL POLYP ( 27 FDA reports)
SPINAL FUSION SURGERY ( 27 FDA reports)
STUPOR ( 27 FDA reports)
VENTRICULAR HYPOKINESIA ( 27 FDA reports)
ABNORMAL SENSATION IN EYE ( 27 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 27 FDA reports)
ALCOHOL USE ( 27 FDA reports)
BLOOD COUNT ABNORMAL ( 27 FDA reports)
BRADYPHRENIA ( 27 FDA reports)
BREAST TENDERNESS ( 27 FDA reports)
BRONCHOSPASM ( 27 FDA reports)
CAROTID ARTERY OCCLUSION ( 27 FDA reports)
EXTRASYSTOLES ( 27 FDA reports)
FURUNCLE ( 27 FDA reports)
HAIR GROWTH ABNORMAL ( 27 FDA reports)
HORDEOLUM ( 27 FDA reports)
INCREASED APPETITE ( 27 FDA reports)
JOINT SPRAIN ( 27 FDA reports)
LIPASE INCREASED ( 27 FDA reports)
MYOPIA ( 27 FDA reports)
NEOPLASM ( 27 FDA reports)
NEPHROGENIC ANAEMIA ( 27 FDA reports)
ORTHOPNOEA ( 27 FDA reports)
PROSTATE CANCER METASTATIC ( 27 FDA reports)
AORTIC STENOSIS ( 26 FDA reports)
AORTIC VALVE SCLEROSIS ( 26 FDA reports)
BLOOD CHLORIDE INCREASED ( 26 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 26 FDA reports)
BREAST RECONSTRUCTION ( 26 FDA reports)
CERVIX CARCINOMA ( 26 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 26 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 26 FDA reports)
EARLY SATIETY ( 26 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 26 FDA reports)
EOSINOPHILIA ( 26 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 26 FDA reports)
GUILLAIN-BARRE SYNDROME ( 26 FDA reports)
HYPOMANIA ( 26 FDA reports)
HYPOTHERMIA ( 26 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 26 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 26 FDA reports)
LUNG HYPERINFLATION ( 26 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 26 FDA reports)
MYASTHENIA GRAVIS ( 26 FDA reports)
NEPHROSCLEROSIS ( 26 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 26 FDA reports)
NEUTROPHIL COUNT INCREASED ( 26 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 26 FDA reports)
OTITIS EXTERNA ( 26 FDA reports)
PERSONALITY CHANGE ( 26 FDA reports)
POLYDIPSIA ( 26 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 26 FDA reports)
PROTEIN URINE ( 26 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 26 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 26 FDA reports)
WOUND SECRETION ( 26 FDA reports)
RADICULAR PAIN ( 25 FDA reports)
RASH PUSTULAR ( 25 FDA reports)
RECTAL FISSURE ( 25 FDA reports)
AMMONIA INCREASED ( 25 FDA reports)
APHTHOUS STOMATITIS ( 25 FDA reports)
BLOOD CREATINE INCREASED ( 25 FDA reports)
BURNS SECOND DEGREE ( 25 FDA reports)
COLON ADENOMA ( 25 FDA reports)
DIASTOLIC DYSFUNCTION ( 25 FDA reports)
DROP ATTACKS ( 25 FDA reports)
ENDOCARDITIS ( 25 FDA reports)
ERYTHEMA MULTIFORME ( 25 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 25 FDA reports)
FRUSTRATION ( 25 FDA reports)
GASTROINTESTINAL INFECTION ( 25 FDA reports)
HYPERTONIA ( 25 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 25 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 25 FDA reports)
ILEUS PARALYTIC ( 25 FDA reports)
IMPLANT SITE INFECTION ( 25 FDA reports)
INITIAL INSOMNIA ( 25 FDA reports)
KETOACIDOSIS ( 25 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 25 FDA reports)
OCCULT BLOOD POSITIVE ( 25 FDA reports)
PANCREATITIS CHRONIC ( 25 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 25 FDA reports)
PROTEIN URINE PRESENT ( 25 FDA reports)
ADJUSTMENT DISORDER ( 24 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 24 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 24 FDA reports)
BILIARY DYSKINESIA ( 24 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 24 FDA reports)
BLEPHAROSPASM ( 24 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 24 FDA reports)
BLOOD CULTURE POSITIVE ( 24 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 24 FDA reports)
CATHETER RELATED COMPLICATION ( 24 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 24 FDA reports)
CLAVICLE FRACTURE ( 24 FDA reports)
COELIAC DISEASE ( 24 FDA reports)
COMMUNICATION DISORDER ( 24 FDA reports)
CONVERSION DISORDER ( 24 FDA reports)
DEVICE OCCLUSION ( 24 FDA reports)
DRUG EFFECT INCREASED ( 24 FDA reports)
ENURESIS ( 24 FDA reports)
FOLLICULITIS ( 24 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 24 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 24 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 24 FDA reports)
GUN SHOT WOUND ( 24 FDA reports)
HEPATITIS B ( 24 FDA reports)
HYPERVENTILATION ( 24 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 24 FDA reports)
LIGAMENT RUPTURE ( 24 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 24 FDA reports)
MULTIPLE FRACTURES ( 24 FDA reports)
NEPHROPATHY ( 24 FDA reports)
OESOPHAGEAL ULCER ( 24 FDA reports)
OLIGURIA ( 24 FDA reports)
PAROSMIA ( 24 FDA reports)
PRODUCT TASTE ABNORMAL ( 24 FDA reports)
PROTEIN TOTAL INCREASED ( 24 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 24 FDA reports)
RADIATION ASSOCIATED PAIN ( 24 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 24 FDA reports)
SEBORRHOEIC DERMATITIS ( 24 FDA reports)
SELF-MEDICATION ( 24 FDA reports)
SKIN PLAQUE ( 24 FDA reports)
STRESS FRACTURE ( 24 FDA reports)
TENDON RUPTURE ( 24 FDA reports)
THROMBOPHLEBITIS ( 24 FDA reports)
TOXIC ENCEPHALOPATHY ( 24 FDA reports)
SKIN ODOUR ABNORMAL ( 23 FDA reports)
SOPOR ( 23 FDA reports)
VEIN DISORDER ( 23 FDA reports)
VITAMIN D DECREASED ( 23 FDA reports)
APPLICATION SITE PRURITUS ( 23 FDA reports)
ASTIGMATISM ( 23 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 23 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 23 FDA reports)
BREAST CANCER FEMALE ( 23 FDA reports)
BREATH SOUNDS ABNORMAL ( 23 FDA reports)
BUNDLE BRANCH BLOCK ( 23 FDA reports)
CARDIAC PACEMAKER INSERTION ( 23 FDA reports)
CARDIAC TAMPONADE ( 23 FDA reports)
DYSTHYMIC DISORDER ( 23 FDA reports)
EDENTULOUS ( 23 FDA reports)
ENCEPHALOMALACIA ( 23 FDA reports)
ENTERITIS ( 23 FDA reports)
EXOPHTHALMOS ( 23 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 23 FDA reports)
HYPERACUSIS ( 23 FDA reports)
HYPOREFLEXIA ( 23 FDA reports)
INJECTION SITE URTICARIA ( 23 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 23 FDA reports)
OBSTRUCTIVE UROPATHY ( 23 FDA reports)
OPEN REDUCTION OF FRACTURE ( 23 FDA reports)
OVARIAN CANCER ( 23 FDA reports)
PATELLA FRACTURE ( 23 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 23 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 23 FDA reports)
POLYP ( 23 FDA reports)
PSEUDOMONAS INFECTION ( 23 FDA reports)
ABDOMINAL RIGIDITY ( 22 FDA reports)
ACCIDENTAL DEATH ( 22 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 22 FDA reports)
ADNEXA UTERI MASS ( 22 FDA reports)
ANAL FISSURE ( 22 FDA reports)
ANAPHYLACTIC SHOCK ( 22 FDA reports)
APLASIA PURE RED CELL ( 22 FDA reports)
CUTANEOUS VASCULITIS ( 22 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 22 FDA reports)
DYSPLASIA ( 22 FDA reports)
EXTREMITY CONTRACTURE ( 22 FDA reports)
FLUID INTAKE REDUCED ( 22 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 22 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 22 FDA reports)
HYPERMETABOLISM ( 22 FDA reports)
HYPERPHOSPHATAEMIA ( 22 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 22 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 22 FDA reports)
INJECTION SITE BURNING ( 22 FDA reports)
INJECTION SITE NECROSIS ( 22 FDA reports)
INTERMITTENT CLAUDICATION ( 22 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 22 FDA reports)
LOSS OF LIBIDO ( 22 FDA reports)
MENIERE'S DISEASE ( 22 FDA reports)
MICROANGIOPATHY ( 22 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 22 FDA reports)
OVARIAN CYST ( 22 FDA reports)
PROSTHESIS USER ( 22 FDA reports)
RECTAL ABSCESS ( 22 FDA reports)
REFLUX OESOPHAGITIS ( 22 FDA reports)
SINUS POLYP ( 22 FDA reports)
SKIN NECROSIS ( 22 FDA reports)
STRESS URINARY INCONTINENCE ( 22 FDA reports)
SUICIDAL BEHAVIOUR ( 22 FDA reports)
TELANGIECTASIA ( 22 FDA reports)
THYROID CANCER ( 22 FDA reports)
URETHRAL STENOSIS ( 22 FDA reports)
VERTIGO POSITIONAL ( 22 FDA reports)
VITREOUS DETACHMENT ( 22 FDA reports)
RENAL CELL CARCINOMA ( 21 FDA reports)
SKIN HAEMORRHAGE ( 21 FDA reports)
SKIN IRRITATION ( 21 FDA reports)
SNEEZING ( 21 FDA reports)
SWEAT GLAND DISORDER ( 21 FDA reports)
THERMAL BURN ( 21 FDA reports)
TOOTH EROSION ( 21 FDA reports)
TRACHEAL DEVIATION ( 21 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 21 FDA reports)
ANGIONEUROTIC OEDEMA ( 21 FDA reports)
ARTHRITIS BACTERIAL ( 21 FDA reports)
BLADDER CANCER ( 21 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 21 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 21 FDA reports)
CARDIOPULMONARY FAILURE ( 21 FDA reports)
COLOSTOMY ( 21 FDA reports)
CYSTITIS HAEMORRHAGIC ( 21 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 21 FDA reports)
DISSOCIATION ( 21 FDA reports)
FUNGAL SKIN INFECTION ( 21 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 21 FDA reports)
HAEMORRHAGIC ANAEMIA ( 21 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 21 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 21 FDA reports)
INJECTION SITE INDURATION ( 21 FDA reports)
KLEBSIELLA INFECTION ( 21 FDA reports)
KNEE OPERATION ( 21 FDA reports)
LUNG CANCER METASTATIC ( 21 FDA reports)
MODERATE MENTAL RETARDATION ( 21 FDA reports)
NAIL DYSTROPHY ( 21 FDA reports)
NASAL POLYPS ( 21 FDA reports)
NEUROLOGICAL SYMPTOM ( 21 FDA reports)
OSTEOMA ( 21 FDA reports)
OVERWEIGHT ( 21 FDA reports)
PARONYCHIA ( 21 FDA reports)
PNEUMONIA BACTERIAL ( 21 FDA reports)
POST LAMINECTOMY SYNDROME ( 21 FDA reports)
PRIAPISM ( 21 FDA reports)
PULMONARY GRANULOMA ( 21 FDA reports)
ALCOHOL POISONING ( 20 FDA reports)
ALCOHOLISM ( 20 FDA reports)
AORTIC VALVE DISEASE ( 20 FDA reports)
BACTERIAL TEST POSITIVE ( 20 FDA reports)
CACHEXIA ( 20 FDA reports)
CERVICOBRACHIAL SYNDROME ( 20 FDA reports)
COLITIS ULCERATIVE ( 20 FDA reports)
CUSHING'S SYNDROME ( 20 FDA reports)
DROOLING ( 20 FDA reports)
DRUG TOLERANCE ( 20 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 20 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 20 FDA reports)
EXCESSIVE EYE BLINKING ( 20 FDA reports)
EYE DISCHARGE ( 20 FDA reports)
FAMILY STRESS ( 20 FDA reports)
GINGIVAL OEDEMA ( 20 FDA reports)
GLARE ( 20 FDA reports)
HICCUPS ( 20 FDA reports)
HYPERBILIRUBINAEMIA ( 20 FDA reports)
HYPOALBUMINAEMIA ( 20 FDA reports)
INJECTION SITE INFECTION ( 20 FDA reports)
INTENTIONAL SELF-INJURY ( 20 FDA reports)
ISCHAEMIC STROKE ( 20 FDA reports)
JAUNDICE CHOLESTATIC ( 20 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 20 FDA reports)
LIVEDO RETICULARIS ( 20 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 20 FDA reports)
MELANOSIS COLI ( 20 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 20 FDA reports)
MOUTH HAEMORRHAGE ( 20 FDA reports)
NARCOTIC INTOXICATION ( 20 FDA reports)
OESOPHAGITIS ULCERATIVE ( 20 FDA reports)
PAPILLOMA ( 20 FDA reports)
PERSONALITY DISORDER ( 20 FDA reports)
POISONING DELIBERATE ( 20 FDA reports)
POOR VENOUS ACCESS ( 20 FDA reports)
PULMONARY HAEMORRHAGE ( 20 FDA reports)
RADICULITIS ( 20 FDA reports)
RENAL CANCER ( 20 FDA reports)
RENAL MASS ( 20 FDA reports)
SACROILIITIS ( 20 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 20 FDA reports)
TOBACCO ABUSE ( 20 FDA reports)
URINE COLOUR ABNORMAL ( 20 FDA reports)
VENTRICULAR ARRHYTHMIA ( 20 FDA reports)
VITAMIN B12 INCREASED ( 20 FDA reports)
RETINAL DEPOSITS ( 19 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 19 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 19 FDA reports)
STAPHYLOMA ( 19 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 19 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 19 FDA reports)
TRANSFUSION ( 19 FDA reports)
UNDERDOSE ( 19 FDA reports)
VASCULAR CALCIFICATION ( 19 FDA reports)
VENOUS THROMBOSIS LIMB ( 19 FDA reports)
ACETABULUM FRACTURE ( 19 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 19 FDA reports)
ACUTE PRERENAL FAILURE ( 19 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 19 FDA reports)
ANXIETY DISORDER ( 19 FDA reports)
APPLICATION SITE IRRITATION ( 19 FDA reports)
APPLICATION SITE VESICLES ( 19 FDA reports)
ATRIAL TACHYCARDIA ( 19 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 19 FDA reports)
BLOOD PH DECREASED ( 19 FDA reports)
BONE FRAGMENTATION ( 19 FDA reports)
BONE MARROW TRANSPLANT ( 19 FDA reports)
CHOLECYSTITIS ACUTE ( 19 FDA reports)
CHONDROPATHY ( 19 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 19 FDA reports)
DRY THROAT ( 19 FDA reports)
DUODENAL ULCER ( 19 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 19 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 19 FDA reports)
ENDOMETRIOSIS ( 19 FDA reports)
ENDOTRACHEAL INTUBATION ( 19 FDA reports)
EXFOLIATIVE RASH ( 19 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 19 FDA reports)
FRACTURED SACRUM ( 19 FDA reports)
GRIMACING ( 19 FDA reports)
IMPULSE-CONTROL DISORDER ( 19 FDA reports)
INFECTED SKIN ULCER ( 19 FDA reports)
INTESTINAL ISCHAEMIA ( 19 FDA reports)
KYPHOSCOLIOSIS ( 19 FDA reports)
LICHENOID KERATOSIS ( 19 FDA reports)
MECHANICAL VENTILATION ( 19 FDA reports)
MENOPAUSE ( 19 FDA reports)
METABOLIC DISORDER ( 19 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 19 FDA reports)
MONOCYTOSIS ( 19 FDA reports)
NON-CARDIAC CHEST PAIN ( 19 FDA reports)
OCULAR HYPERTENSION ( 19 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 19 FDA reports)
OSTEOCHONDROSIS ( 19 FDA reports)
PANCREATIC CARCINOMA ( 19 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 19 FDA reports)
POSTNASAL DRIP ( 19 FDA reports)
PROSTATITIS ( 19 FDA reports)
ABSCESS NECK ( 18 FDA reports)
ABSCESS ORAL ( 18 FDA reports)
ANOSMIA ( 18 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 18 FDA reports)
AORTIC DILATATION ( 18 FDA reports)
APPARENT DEATH ( 18 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 18 FDA reports)
BLADDER PROLAPSE ( 18 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 18 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 18 FDA reports)
CUBITAL TUNNEL SYNDROME ( 18 FDA reports)
DEAFNESS UNILATERAL ( 18 FDA reports)
DIABETIC COMPLICATION ( 18 FDA reports)
DYSPHASIA ( 18 FDA reports)
EXTERNAL EAR DISORDER ( 18 FDA reports)
EYELID FUNCTION DISORDER ( 18 FDA reports)
FACIAL PARESIS ( 18 FDA reports)
FEELING OF DESPAIR ( 18 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 18 FDA reports)
FOOD INTOLERANCE ( 18 FDA reports)
GINGIVAL EROSION ( 18 FDA reports)
HYPERMETROPIA ( 18 FDA reports)
IMMUNODEFICIENCY ( 18 FDA reports)
INJECTION SITE DISCOLOURATION ( 18 FDA reports)
IRITIS ( 18 FDA reports)
MAXILLOFACIAL OPERATION ( 18 FDA reports)
MENSTRUATION IRREGULAR ( 18 FDA reports)
METASTASES TO LYMPH NODES ( 18 FDA reports)
MONOPLEGIA ( 18 FDA reports)
MUSCLE INJURY ( 18 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 18 FDA reports)
PANCREATIC DISORDER ( 18 FDA reports)
PANIC DISORDER ( 18 FDA reports)
PAPILLOEDEMA ( 18 FDA reports)
PELVIC ABSCESS ( 18 FDA reports)
PYODERMA GANGRENOSUM ( 18 FDA reports)
RESPIRATION ABNORMAL ( 18 FDA reports)
SCIATIC NERVE INJURY ( 18 FDA reports)
SJOGREN'S SYNDROME ( 18 FDA reports)
SKIN INFECTION ( 18 FDA reports)
SPONDYLITIS ( 18 FDA reports)
STASIS DERMATITIS ( 18 FDA reports)
TENOSYNOVITIS ( 18 FDA reports)
THROMBOCYTOSIS ( 18 FDA reports)
THROMBOSIS IN DEVICE ( 18 FDA reports)
TONGUE BITING ( 18 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 18 FDA reports)
TRIGGER FINGER ( 18 FDA reports)
UPPER EXTREMITY MASS ( 18 FDA reports)
VITAMIN B12 DEFICIENCY ( 18 FDA reports)
STARING ( 17 FDA reports)
TONGUE OEDEMA ( 17 FDA reports)
ULNAR NEURITIS ( 17 FDA reports)
VENA CAVA THROMBOSIS ( 17 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 17 FDA reports)
ABDOMINAL ADHESIONS ( 17 FDA reports)
ANION GAP INCREASED ( 17 FDA reports)
APPENDICECTOMY ( 17 FDA reports)
APPENDICITIS PERFORATED ( 17 FDA reports)
BILIARY COLIC ( 17 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 17 FDA reports)
BLOOD LACTIC ACID INCREASED ( 17 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 17 FDA reports)
CARDIAC VALVE SCLEROSIS ( 17 FDA reports)
CLAUSTROPHOBIA ( 17 FDA reports)
COLON OPERATION ( 17 FDA reports)
COLOUR BLINDNESS ( 17 FDA reports)
CONDUCTION DISORDER ( 17 FDA reports)
CORNEAL DYSTROPHY ( 17 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 17 FDA reports)
DEPRESSIVE SYMPTOM ( 17 FDA reports)
DIZZINESS POSTURAL ( 17 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 17 FDA reports)
EJACULATION FAILURE ( 17 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 17 FDA reports)
FOLATE DEFICIENCY ( 17 FDA reports)
GINGIVAL ABSCESS ( 17 FDA reports)
GRAFT VERSUS HOST DISEASE ( 17 FDA reports)
HAEMORRHAGIC STROKE ( 17 FDA reports)
HEAD TITUBATION ( 17 FDA reports)
HEARING AID USER ( 17 FDA reports)
HEAT EXHAUSTION ( 17 FDA reports)
HEPATIC CONGESTION ( 17 FDA reports)
HODGKIN'S DISEASE ( 17 FDA reports)
HYDROCEPHALUS ( 17 FDA reports)
HYPERAMYLASAEMIA ( 17 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 17 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 17 FDA reports)
INJECTION SITE EXTRAVASATION ( 17 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 17 FDA reports)
KIDNEY SMALL ( 17 FDA reports)
LIMB CRUSHING INJURY ( 17 FDA reports)
LOCALISED OEDEMA ( 17 FDA reports)
LOWER EXTREMITY MASS ( 17 FDA reports)
MALIGNANT MELANOMA IN SITU ( 17 FDA reports)
MASTITIS ( 17 FDA reports)
MITRAL VALVE CALCIFICATION ( 17 FDA reports)
NEURODERMATITIS ( 17 FDA reports)
NODULE ON EXTREMITY ( 17 FDA reports)
NON-SMALL CELL LUNG CANCER ( 17 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 17 FDA reports)
OESOPHAGEAL STENOSIS ( 17 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 17 FDA reports)
PITTING OEDEMA ( 17 FDA reports)
PLASTIC SURGERY ( 17 FDA reports)
PO2 DECREASED ( 17 FDA reports)
PROSTATOMEGALY ( 17 FDA reports)
PULMONARY RADIATION INJURY ( 17 FDA reports)
ACUTE PULMONARY OEDEMA ( 16 FDA reports)
AMYLOIDOSIS ( 16 FDA reports)
ANGIOFIBROMA ( 16 FDA reports)
BLADDER PAIN ( 16 FDA reports)
BLEPHARITIS ( 16 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 16 FDA reports)
BONE FISSURE ( 16 FDA reports)
BONE FISTULA ( 16 FDA reports)
BREAKTHROUGH PAIN ( 16 FDA reports)
BREAST CYST ( 16 FDA reports)
CALCINOSIS ( 16 FDA reports)
CARDIOTOXICITY ( 16 FDA reports)
CATARACT NUCLEAR ( 16 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 16 FDA reports)
CHEST WALL MASS ( 16 FDA reports)
CHEST WALL OPERATION ( 16 FDA reports)
CHOLECYSTITIS INFECTIVE ( 16 FDA reports)
CONJUNCTIVOCHALASIS ( 16 FDA reports)
CONNECTIVE TISSUE DISORDER ( 16 FDA reports)
EAR DISORDER ( 16 FDA reports)
EROSIVE DUODENITIS ( 16 FDA reports)
FIBRIN D DIMER INCREASED ( 16 FDA reports)
FOETAL MONITORING ABNORMAL ( 16 FDA reports)
FOOD POISONING ( 16 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 16 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 16 FDA reports)
HAEMANGIOMA OF SKIN ( 16 FDA reports)
HERNIA REPAIR ( 16 FDA reports)
INJECTION SITE OEDEMA ( 16 FDA reports)
INTERTRIGO ( 16 FDA reports)
INTESTINAL DILATATION ( 16 FDA reports)
INTRAOCULAR LENS IMPLANT ( 16 FDA reports)
JOINT LOCK ( 16 FDA reports)
JUDGEMENT IMPAIRED ( 16 FDA reports)
KERATITIS ( 16 FDA reports)
LIP DISORDER ( 16 FDA reports)
LISTLESS ( 16 FDA reports)
MACULE ( 16 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 16 FDA reports)
METASTASES TO ADRENALS ( 16 FDA reports)
MICTURITION DISORDER ( 16 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 16 FDA reports)
MOANING ( 16 FDA reports)
MUCOSAL DRYNESS ( 16 FDA reports)
MYOCLONIC EPILEPSY ( 16 FDA reports)
NEPHROPATHY TOXIC ( 16 FDA reports)
OPHTHALMOPLEGIA ( 16 FDA reports)
OSTEOMYELITIS CHRONIC ( 16 FDA reports)
OVARIAN MASS ( 16 FDA reports)
PARAPARESIS ( 16 FDA reports)
PEPTIC ULCER ( 16 FDA reports)
PERIARTHRITIS ( 16 FDA reports)
PERICARDITIS ( 16 FDA reports)
PERIORBITAL OEDEMA ( 16 FDA reports)
PHANTOM PAIN ( 16 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 16 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 16 FDA reports)
PROCTITIS ( 16 FDA reports)
PROLAPSE REPAIR ( 16 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 16 FDA reports)
RETINAL TEAR ( 16 FDA reports)
RHINALGIA ( 16 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 16 FDA reports)
SENSATION OF PRESSURE ( 16 FDA reports)
SHOULDER PAIN ( 16 FDA reports)
SKIN CANDIDA ( 16 FDA reports)
SKIN WARM ( 16 FDA reports)
SOCIAL PROBLEM ( 16 FDA reports)
STREPTOCOCCAL INFECTION ( 16 FDA reports)
TALIPES ( 16 FDA reports)
TOE AMPUTATION ( 16 FDA reports)
TOOTH IMPACTED ( 16 FDA reports)
TREATMENT FAILURE ( 16 FDA reports)
VERBAL ABUSE ( 16 FDA reports)
PUPILS UNEQUAL ( 15 FDA reports)
RECTAL PROLAPSE ( 15 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 15 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 15 FDA reports)
SPINAL CORD INJURY ( 15 FDA reports)
SPINAL DEFORMITY ( 15 FDA reports)
SPLENIC LESION ( 15 FDA reports)
SPONDYLOLYSIS ( 15 FDA reports)
SYNOVITIS ( 15 FDA reports)
TOOTH INJURY ( 15 FDA reports)
ULCER HAEMORRHAGE ( 15 FDA reports)
UMBILICAL HERNIA ( 15 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 15 FDA reports)
URINARY TRACT DISORDER ( 15 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 15 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 15 FDA reports)
VULVOVAGINAL DRYNESS ( 15 FDA reports)
ABSCESS LIMB ( 15 FDA reports)
ADRENAL ADENOMA ( 15 FDA reports)
APPLICATION SITE PAIN ( 15 FDA reports)
ARTERIAL DISORDER ( 15 FDA reports)
ATROPHIC VULVOVAGINITIS ( 15 FDA reports)
BILE DUCT STONE ( 15 FDA reports)
BLADDER CYST ( 15 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 15 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 15 FDA reports)
BLOOD TEST ABNORMAL ( 15 FDA reports)
BRADYKINESIA ( 15 FDA reports)
BRAIN HERNIATION ( 15 FDA reports)
CALCIUM DEFICIENCY ( 15 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 15 FDA reports)
CHEILITIS ( 15 FDA reports)
COLON POLYPECTOMY ( 15 FDA reports)
DIABETES INSIPIDUS ( 15 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 15 FDA reports)
EMBOLISM ( 15 FDA reports)
FEAR OF WEIGHT GAIN ( 15 FDA reports)
FIBROUS HISTIOCYTOMA ( 15 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 15 FDA reports)
HAEMODYNAMIC INSTABILITY ( 15 FDA reports)
HALLUCINATIONS, MIXED ( 15 FDA reports)
HEAD DISCOMFORT ( 15 FDA reports)
HEPATOSPLENOMEGALY ( 15 FDA reports)
HOMICIDE ( 15 FDA reports)
HYDROCELE ( 15 FDA reports)
IATROGENIC INJURY ( 15 FDA reports)
IMMOBILE ( 15 FDA reports)
INCISIONAL DRAINAGE ( 15 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 15 FDA reports)
KLEBSIELLA TEST POSITIVE ( 15 FDA reports)
LIP HAEMORRHAGE ( 15 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 15 FDA reports)
MEAN CELL VOLUME INCREASED ( 15 FDA reports)
MENINGIOMA ( 15 FDA reports)
METASTASES TO LARGE INTESTINE ( 15 FDA reports)
NEUROPATHIC PAIN ( 15 FDA reports)
NICOTINE DEPENDENCE ( 15 FDA reports)
PAINFUL RESPIRATION ( 15 FDA reports)
PARTNER STRESS ( 15 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 15 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 15 FDA reports)
PRINZMETAL ANGINA ( 15 FDA reports)
PRODUCT ODOUR ABNORMAL ( 15 FDA reports)
PSYCHOMOTOR RETARDATION ( 15 FDA reports)
PULMONARY INFARCTION ( 15 FDA reports)
PULSE PRESSURE DECREASED ( 15 FDA reports)
ADRENAL DISORDER ( 14 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 14 FDA reports)
ALCOHOL ABUSE ( 14 FDA reports)
ALVEOLAR OSTEITIS ( 14 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 14 FDA reports)
APRAXIA ( 14 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 14 FDA reports)
BLOOD PH INCREASED ( 14 FDA reports)
BRONCHITIS ACUTE ( 14 FDA reports)
CARTILAGE INJURY ( 14 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 14 FDA reports)
CEREBELLAR SYNDROME ( 14 FDA reports)
COLPOCELE ( 14 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 14 FDA reports)
CORNEAL ABRASION ( 14 FDA reports)
CUSHINGOID ( 14 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 14 FDA reports)
DENTAL OPERATION ( 14 FDA reports)
DERMATITIS ALLERGIC ( 14 FDA reports)
DUODENITIS ( 14 FDA reports)
DYSPLASTIC NAEVUS ( 14 FDA reports)
FLAT AFFECT ( 14 FDA reports)
FULL BLOOD COUNT DECREASED ( 14 FDA reports)
GINGIVAL ERYTHEMA ( 14 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 14 FDA reports)
HAEMOTHORAX ( 14 FDA reports)
HAND DEFORMITY ( 14 FDA reports)
HEART RATE ABNORMAL ( 14 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 14 FDA reports)
HYPERAMMONAEMIA ( 14 FDA reports)
HYPOGEUSIA ( 14 FDA reports)
HYPOPROTEINAEMIA ( 14 FDA reports)
INAPPROPRIATE AFFECT ( 14 FDA reports)
INCORRECT STORAGE OF DRUG ( 14 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 14 FDA reports)
INTESTINAL MASS ( 14 FDA reports)
INTRACRANIAL HYPOTENSION ( 14 FDA reports)
LACTOSE INTOLERANCE ( 14 FDA reports)
LARGE INTESTINAL ULCER ( 14 FDA reports)
LERICHE SYNDROME ( 14 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 14 FDA reports)
MEDICAL DEVICE REMOVAL ( 14 FDA reports)
METASTASES TO PLEURA ( 14 FDA reports)
METASTASIS ( 14 FDA reports)
MICTURITION FREQUENCY DECREASED ( 14 FDA reports)
MOUTH INJURY ( 14 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 14 FDA reports)
MYELOMA RECURRENCE ( 14 FDA reports)
NEPHROTIC SYNDROME ( 14 FDA reports)
NERVE ROOT COMPRESSION ( 14 FDA reports)
OCCIPITAL NEURALGIA ( 14 FDA reports)
OCULAR ICTERUS ( 14 FDA reports)
OESOPHAGEAL PAIN ( 14 FDA reports)
OESOPHAGEAL SPASM ( 14 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 14 FDA reports)
OROPHARYNGEAL BLISTERING ( 14 FDA reports)
PERITONITIS BACTERIAL ( 14 FDA reports)
POLYARTHRITIS ( 14 FDA reports)
POST PROCEDURAL INFECTION ( 14 FDA reports)
PUPIL FIXED ( 14 FDA reports)
PYELONEPHRITIS ACUTE ( 14 FDA reports)
RESPIRATORY ALKALOSIS ( 14 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 14 FDA reports)
ROTATOR CUFF REPAIR ( 14 FDA reports)
SKIN REACTION ( 14 FDA reports)
SPINAL CORD DISORDER ( 14 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 14 FDA reports)
TEARFULNESS ( 14 FDA reports)
TOOTH DISCOLOURATION ( 14 FDA reports)
VAGINAL PROLAPSE ( 14 FDA reports)
VENOUS INSUFFICIENCY ( 14 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 14 FDA reports)
RENAL TRANSPLANT ( 13 FDA reports)
RESIDUAL URINE ( 13 FDA reports)
RETICULOCYTE COUNT INCREASED ( 13 FDA reports)
RETINOPATHY ( 13 FDA reports)
SALIVA ALTERED ( 13 FDA reports)
SELF ESTEEM DECREASED ( 13 FDA reports)
SERUM SICKNESS ( 13 FDA reports)
SKIN FISSURES ( 13 FDA reports)
SKULL FRACTURE ( 13 FDA reports)
SKULL MALFORMATION ( 13 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 13 FDA reports)
SPUTUM CULTURE POSITIVE ( 13 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 13 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 13 FDA reports)
TENOSYNOVITIS STENOSANS ( 13 FDA reports)
TOOTH REPAIR ( 13 FDA reports)
TRACHEOBRONCHITIS ( 13 FDA reports)
VASCULAR OCCLUSION ( 13 FDA reports)
VASCULITIC RASH ( 13 FDA reports)
VENTRICULAR DYSKINESIA ( 13 FDA reports)
WOUND HAEMORRHAGE ( 13 FDA reports)
ACANTHOMA ( 13 FDA reports)
ACARODERMATITIS ( 13 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 13 FDA reports)
ADENOMA BENIGN ( 13 FDA reports)
ALLODYNIA ( 13 FDA reports)
ANAL SKIN TAGS ( 13 FDA reports)
ANIMAL BITE ( 13 FDA reports)
ATROPHY ( 13 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 13 FDA reports)
BENIGN OVARIAN TUMOUR ( 13 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 13 FDA reports)
BIOPSY GINGIVAL ( 13 FDA reports)
BIPOLAR I DISORDER ( 13 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 13 FDA reports)
BONE SCAN ABNORMAL ( 13 FDA reports)
BRAIN SCAN ABNORMAL ( 13 FDA reports)
BULLOUS LUNG DISEASE ( 13 FDA reports)
CARDIAC ANEURYSM ( 13 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 13 FDA reports)
CATATONIA ( 13 FDA reports)
CEREBRAL CYST ( 13 FDA reports)
CEREBROVASCULAR DISORDER ( 13 FDA reports)
CERVICAL CORD COMPRESSION ( 13 FDA reports)
COSTOCHONDRITIS ( 13 FDA reports)
CYSTOSCOPY ( 13 FDA reports)
CYTOLYTIC HEPATITIS ( 13 FDA reports)
DERMATITIS BULLOUS ( 13 FDA reports)
DEVICE BREAKAGE ( 13 FDA reports)
DYSPHORIA ( 13 FDA reports)
EAR HAEMORRHAGE ( 13 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 13 FDA reports)
EMPYEMA ( 13 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 13 FDA reports)
ENTEROVESICAL FISTULA ( 13 FDA reports)
EXERCISE TOLERANCE DECREASED ( 13 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 13 FDA reports)
GLIOSIS ( 13 FDA reports)
HAEMORRHOID OPERATION ( 13 FDA reports)
HEART INJURY ( 13 FDA reports)
HYPERCHLORHYDRIA ( 13 FDA reports)
IMMUNOSUPPRESSION ( 13 FDA reports)
INJECTION SITE INFLAMMATION ( 13 FDA reports)
INJECTION SITE NODULE ( 13 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 13 FDA reports)
JOINT ARTHROPLASTY ( 13 FDA reports)
KERATOMILEUSIS ( 13 FDA reports)
LABILE BLOOD PRESSURE ( 13 FDA reports)
LIGAMENT INJURY ( 13 FDA reports)
LOGORRHOEA ( 13 FDA reports)
MACULAR OEDEMA ( 13 FDA reports)
MALLORY-WEISS SYNDROME ( 13 FDA reports)
MARITAL PROBLEM ( 13 FDA reports)
MASTOIDITIS ( 13 FDA reports)
METAPLASIA ( 13 FDA reports)
MONONUCLEOSIS SYNDROME ( 13 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 13 FDA reports)
MORTON'S NEUROMA ( 13 FDA reports)
MULTIPLE ALLERGIES ( 13 FDA reports)
MYELOMALACIA ( 13 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 13 FDA reports)
NAIL DISCOLOURATION ( 13 FDA reports)
NEPHRITIS INTERSTITIAL ( 13 FDA reports)
NEUROFIBROMA ( 13 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 13 FDA reports)
OSTEORADIONECROSIS ( 13 FDA reports)
PAROTID GLAND ENLARGEMENT ( 13 FDA reports)
PCO2 DECREASED ( 13 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 13 FDA reports)
PILOERECTION ( 13 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 13 FDA reports)
PROSTATISM ( 13 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 13 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 13 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 13 FDA reports)
PULMONARY THROMBOSIS ( 13 FDA reports)
ACUTE PSYCHOSIS ( 12 FDA reports)
AGORAPHOBIA ( 12 FDA reports)
APPLICATION SITE BURN ( 12 FDA reports)
ATHEROSCLEROSIS ( 12 FDA reports)
ATRIAL SEPTAL DEFECT ( 12 FDA reports)
AUTOIMMUNE DISORDER ( 12 FDA reports)
AXONAL NEUROPATHY ( 12 FDA reports)
B-CELL LYMPHOMA ( 12 FDA reports)
BIOPSY LIVER ( 12 FDA reports)
BLOOD BLISTER ( 12 FDA reports)
BLOOD CORTISOL ABNORMAL ( 12 FDA reports)
BLOOD FOLATE INCREASED ( 12 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 12 FDA reports)
BONE GIANT CELL TUMOUR ( 12 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 12 FDA reports)
CALCIPHYLAXIS ( 12 FDA reports)
CANCER PAIN ( 12 FDA reports)
CARDIAC FAILURE CHRONIC ( 12 FDA reports)
CARDIAC FLUTTER ( 12 FDA reports)
CHOKING SENSATION ( 12 FDA reports)
CHOLESTEATOMA ( 12 FDA reports)
COLONOSCOPY ( 12 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 12 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 12 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 12 FDA reports)
DISTRACTIBILITY ( 12 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 12 FDA reports)
EMBOLISM VENOUS ( 12 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 12 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR DECREASED ( 12 FDA reports)
ESCHERICHIA SEPSIS ( 12 FDA reports)
FEAR OF DEATH ( 12 FDA reports)
FOREIGN BODY TRAUMA ( 12 FDA reports)
GRAM STAIN ( 12 FDA reports)
HAEMATOCRIT INCREASED ( 12 FDA reports)
HANGOVER ( 12 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 12 FDA reports)
ILIAC ARTERY THROMBOSIS ( 12 FDA reports)
ILIUM FRACTURE ( 12 FDA reports)
INFARCTION ( 12 FDA reports)
INFUSION SITE PAIN ( 12 FDA reports)
INTERVERTEBRAL DISCITIS ( 12 FDA reports)
INTRACARDIAC THROMBUS ( 12 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 12 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 12 FDA reports)
LUPUS-LIKE SYNDROME ( 12 FDA reports)
MACULAR HOLE ( 12 FDA reports)
MEGACOLON ( 12 FDA reports)
METAL POISONING ( 12 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 12 FDA reports)
MICROCYTIC ANAEMIA ( 12 FDA reports)
MYELOPATHY ( 12 FDA reports)
NAIL OPERATION ( 12 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 12 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 12 FDA reports)
OPEN ANGLE GLAUCOMA ( 12 FDA reports)
ORGAN FAILURE ( 12 FDA reports)
PEAU D'ORANGE ( 12 FDA reports)
PERICARDIAL DISEASE ( 12 FDA reports)
PERIPHERAL EMBOLISM ( 12 FDA reports)
PERITONEAL ADHESIONS ( 12 FDA reports)
PHOBIA ( 12 FDA reports)
PITUITARY TUMOUR BENIGN ( 12 FDA reports)
PNEUMATOSIS INTESTINALIS ( 12 FDA reports)
POLYPECTOMY ( 12 FDA reports)
PRECANCEROUS CELLS PRESENT ( 12 FDA reports)
PREMATURE BABY ( 12 FDA reports)
PREMATURE LABOUR ( 12 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 12 FDA reports)
RADICAL HYSTERECTOMY ( 12 FDA reports)
RAYNAUD'S PHENOMENON ( 12 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 12 FDA reports)
RENAL ANEURYSM ( 12 FDA reports)
RESUSCITATION ( 12 FDA reports)
RETINAL DISORDER ( 12 FDA reports)
RETINITIS ( 12 FDA reports)
RETINOPATHY HYPERTENSIVE ( 12 FDA reports)
RHINOPLASTY ( 12 FDA reports)
RIGHT VENTRICULAR FAILURE ( 12 FDA reports)
SALPINGO-OOPHORECTOMY ( 12 FDA reports)
SINUS POLYP DEGENERATION ( 12 FDA reports)
SKIN NEOPLASM EXCISION ( 12 FDA reports)
SKIN NODULE ( 12 FDA reports)
SPINAL CORPECTOMY ( 12 FDA reports)
SPINAL OPERATION ( 12 FDA reports)
TACHYARRHYTHMIA ( 12 FDA reports)
TENSION ( 12 FDA reports)
THERAPEUTIC PROCEDURE ( 12 FDA reports)
THYROID CYST ( 12 FDA reports)
TOBACCO USER ( 12 FDA reports)
VARICES OESOPHAGEAL ( 12 FDA reports)
VENTRICULAR DYSFUNCTION ( 12 FDA reports)
VESTIBULAR DISORDER ( 12 FDA reports)
VOCAL CORD DISORDER ( 12 FDA reports)
VULVOVAGINITIS ( 12 FDA reports)
YELLOW SKIN ( 12 FDA reports)
RADICULITIS LUMBOSACRAL ( 11 FDA reports)
REGURGITATION ( 11 FDA reports)
RENAL TUBULAR DISORDER ( 11 FDA reports)
RETINAL DETACHMENT ( 11 FDA reports)
SEPSIS SYNDROME ( 11 FDA reports)
SIMPLE PARTIAL SEIZURES ( 11 FDA reports)
SKIN GRAFT ( 11 FDA reports)
SUBSTANCE ABUSE ( 11 FDA reports)
SUDDEN CARDIAC DEATH ( 11 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 11 FDA reports)
SYNOVIAL RUPTURE ( 11 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 11 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 11 FDA reports)
TONSILLITIS ( 11 FDA reports)
TORTICOLLIS ( 11 FDA reports)
TOXIC SKIN ERUPTION ( 11 FDA reports)
TUMOUR NECROSIS ( 11 FDA reports)
URINE ANALYSIS ABNORMAL ( 11 FDA reports)
VAGINAL ULCERATION ( 11 FDA reports)
VASCULAR DEMENTIA ( 11 FDA reports)
VITAMIN B12 DECREASED ( 11 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 11 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 11 FDA reports)
WOUND COMPLICATION ( 11 FDA reports)
YAWNING ( 11 FDA reports)
ADHESION ( 11 FDA reports)
ADVERSE REACTION ( 11 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 11 FDA reports)
ALVEOLITIS ALLERGIC ( 11 FDA reports)
ALVEOLOPLASTY ( 11 FDA reports)
AMNESTIC DISORDER ( 11 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 11 FDA reports)
ASTHENOPIA ( 11 FDA reports)
AURA ( 11 FDA reports)
BARTHOLIN'S CYST ( 11 FDA reports)
BEHCET'S SYNDROME ( 11 FDA reports)
BILE DUCT OBSTRUCTION ( 11 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 11 FDA reports)
BONE MARROW TOXICITY ( 11 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 11 FDA reports)
BRAIN OPERATION ( 11 FDA reports)
BREAST SWELLING ( 11 FDA reports)
BRONCHIOLITIS ( 11 FDA reports)
BUTTOCK PAIN ( 11 FDA reports)
CALCULUS BLADDER ( 11 FDA reports)
CAPILLARY LEAK SYNDROME ( 11 FDA reports)
CARDIAC SEPTAL DEFECT ( 11 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 11 FDA reports)
CAUDA EQUINA SYNDROME ( 11 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 11 FDA reports)
CEREBRAL DISORDER ( 11 FDA reports)
CEREBRAL HAEMATOMA ( 11 FDA reports)
CHOLANGITIS ( 11 FDA reports)
COAGULATION TIME PROLONGED ( 11 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 11 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 11 FDA reports)
CULTURE WOUND POSITIVE ( 11 FDA reports)
CYSTITIS INTERSTITIAL ( 11 FDA reports)
CYSTITIS NONINFECTIVE ( 11 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 11 FDA reports)
DENTAL DISCOMFORT ( 11 FDA reports)
DEVELOPMENTAL DELAY ( 11 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 11 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 11 FDA reports)
ENERGY INCREASED ( 11 FDA reports)
ENGRAFTMENT SYNDROME ( 11 FDA reports)
EPIGASTRIC DISCOMFORT ( 11 FDA reports)
FIBULA FRACTURE ( 11 FDA reports)
FINGER DEFORMITY ( 11 FDA reports)
FOOT AMPUTATION ( 11 FDA reports)
GALLBLADDER OPERATION ( 11 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 11 FDA reports)
HEPATITIS CHOLESTATIC ( 11 FDA reports)
HERPES VIRUS INFECTION ( 11 FDA reports)
HIP SURGERY ( 11 FDA reports)
HYPERTROPHY ( 11 FDA reports)
ILEITIS ( 11 FDA reports)
INCISION SITE INFECTION ( 11 FDA reports)
INDURATION ( 11 FDA reports)
INJECTION SITE CYST ( 11 FDA reports)
INJECTION SITE VESICLES ( 11 FDA reports)
ISCHAEMIC HEPATITIS ( 11 FDA reports)
LEUKOPLAKIA ( 11 FDA reports)
LIP PAIN ( 11 FDA reports)
LOSS OF EMPLOYMENT ( 11 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 11 FDA reports)
MENSTRUAL DISORDER ( 11 FDA reports)
METASTASES TO THORAX ( 11 FDA reports)
METHAEMOGLOBINAEMIA ( 11 FDA reports)
MUCOSAL HAEMORRHAGE ( 11 FDA reports)
NASAL DISORDER ( 11 FDA reports)
NEUROPATHIC ULCER ( 11 FDA reports)
NEUTROPENIC COLITIS ( 11 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 11 FDA reports)
ORAL FIBROMA ( 11 FDA reports)
OVARIAN DISORDER ( 11 FDA reports)
PARAPSORIASIS ( 11 FDA reports)
PATHOGEN RESISTANCE ( 11 FDA reports)
PROTRUSION TONGUE ( 11 FDA reports)
ABNORMAL FAECES ( 10 FDA reports)
APPLICATION SITE REACTION ( 10 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 10 FDA reports)
BLOOD SODIUM INCREASED ( 10 FDA reports)
BREAST ABSCESS ( 10 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 10 FDA reports)
CARBON DIOXIDE DECREASED ( 10 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 10 FDA reports)
CATHETER SITE HAEMATOMA ( 10 FDA reports)
CEREBELLAR ATAXIA ( 10 FDA reports)
CEREBRAL MICROANGIOPATHY ( 10 FDA reports)
CLEFT PALATE ( 10 FDA reports)
CLONUS ( 10 FDA reports)
COR PULMONALE ( 10 FDA reports)
CSF TEST ABNORMAL ( 10 FDA reports)
CYSTOPEXY ( 10 FDA reports)
DEVICE LEAKAGE ( 10 FDA reports)
DEVICE RELATED SEPSIS ( 10 FDA reports)
DIABETIC GASTROPARESIS ( 10 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 10 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 10 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 10 FDA reports)
ENDOMETRIAL CANCER ( 10 FDA reports)
ENDOSCOPY ( 10 FDA reports)
ERYTHEMA OF EYELID ( 10 FDA reports)
ESCHERICHIA TEST POSITIVE ( 10 FDA reports)
EYE OPERATION ( 10 FDA reports)
EYE ROLLING ( 10 FDA reports)
GALLBLADDER INJURY ( 10 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 10 FDA reports)
HELICOBACTER INFECTION ( 10 FDA reports)
HEPATITIS ACUTE ( 10 FDA reports)
HEPATITIS TOXIC ( 10 FDA reports)
HEPATORENAL SYNDROME ( 10 FDA reports)
HYPERCOAGULATION ( 10 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 10 FDA reports)
HYPERTHYROIDISM ( 10 FDA reports)
HYPERURICAEMIA ( 10 FDA reports)
INFUSION SITE HAEMATOMA ( 10 FDA reports)
INJECTION SITE BRUISING ( 10 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 10 FDA reports)
INTERCOSTAL NEURALGIA ( 10 FDA reports)
INTESTINAL HAEMORRHAGE ( 10 FDA reports)
LIGAMENT DISORDER ( 10 FDA reports)
LIP DISCOLOURATION ( 10 FDA reports)
LIP DRY ( 10 FDA reports)
MERALGIA PARAESTHETICA ( 10 FDA reports)
METRORRHAGIA ( 10 FDA reports)
MUMPS ( 10 FDA reports)
MUSCLE CRAMP ( 10 FDA reports)
MUTISM ( 10 FDA reports)
MYELITIS ( 10 FDA reports)
NAIL HYPERTROPHY ( 10 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 10 FDA reports)
NERVE ROOT LESION ( 10 FDA reports)
NEUROPATHIC ARTHROPATHY ( 10 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 10 FDA reports)
OSTEOPOROTIC FRACTURE ( 10 FDA reports)
PARATHYROID TUMOUR BENIGN ( 10 FDA reports)
PARESIS ( 10 FDA reports)
PCO2 INCREASED ( 10 FDA reports)
PHARYNGEAL ERYTHEMA ( 10 FDA reports)
PINGUECULA ( 10 FDA reports)
POOR PERSONAL HYGIENE ( 10 FDA reports)
PORTAL HYPERTENSION ( 10 FDA reports)
POSTOPERATIVE INFECTION ( 10 FDA reports)
PROSTATIC DISORDER ( 10 FDA reports)
PULSE ABNORMAL ( 10 FDA reports)
QUADRIPARESIS ( 10 FDA reports)
RASH MORBILLIFORM ( 10 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 10 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 10 FDA reports)
ROSACEA ( 10 FDA reports)
SALIVARY GLAND PAIN ( 10 FDA reports)
SCLERODERMA ( 10 FDA reports)
SHOULDER OPERATION ( 10 FDA reports)
SINUS ANTROSTOMY ( 10 FDA reports)
SKIN MASS ( 10 FDA reports)
SPINAL HAEMANGIOMA ( 10 FDA reports)
SPLEEN DISORDER ( 10 FDA reports)
SPLENECTOMY ( 10 FDA reports)
SPUTUM PURULENT ( 10 FDA reports)
SUDDEN ONSET OF SLEEP ( 10 FDA reports)
SUPERINFECTION ( 10 FDA reports)
TARSAL TUNNEL SYNDROME ( 10 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 10 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 10 FDA reports)
ULNA FRACTURE ( 10 FDA reports)
URETERIC OBSTRUCTION ( 10 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 10 FDA reports)
UTERINE CANCER ( 10 FDA reports)
UTERINE PROLAPSE REPAIR ( 10 FDA reports)
VASCULAR ANOMALY ( 10 FDA reports)
VASCULAR COMPRESSION ( 10 FDA reports)
WEIGHT BEARING DIFFICULTY ( 10 FDA reports)
WOUND TREATMENT ( 10 FDA reports)
XEROSIS ( 10 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 9 FDA reports)
RUBELLA ( 9 FDA reports)
SARCOIDOSIS ( 9 FDA reports)
SARCOMA ( 9 FDA reports)
SCARLET FEVER ( 9 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 9 FDA reports)
SCROTAL IRRITATION ( 9 FDA reports)
SECRETION DISCHARGE ( 9 FDA reports)
SELF-INJURIOUS IDEATION ( 9 FDA reports)
SHOCK HAEMORRHAGIC ( 9 FDA reports)
SHOULDER DEFORMITY ( 9 FDA reports)
SKIN INJURY ( 9 FDA reports)
SOMATOFORM DISORDER ( 9 FDA reports)
SPONDYLOPATHY TRAUMATIC ( 9 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 9 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 9 FDA reports)
THORACOTOMY ( 9 FDA reports)
TIC ( 9 FDA reports)
TINEA PEDIS ( 9 FDA reports)
TRACHEOSTOMY ( 9 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 9 FDA reports)
URINE OSMOLARITY DECREASED ( 9 FDA reports)
VASCULAR PSEUDOANEURYSM ( 9 FDA reports)
VASOSPASM ( 9 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 9 FDA reports)
VOCAL CORD PARALYSIS ( 9 FDA reports)
ABDOMINAL ABSCESS ( 9 FDA reports)
ABDOMINAL SEPSIS ( 9 FDA reports)
ACCIDENT AT WORK ( 9 FDA reports)
ADRENAL NEOPLASM ( 9 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 9 FDA reports)
ANAEMIA MACROCYTIC ( 9 FDA reports)
ANAL FISSURE EXCISION ( 9 FDA reports)
ANAL PRURITUS ( 9 FDA reports)
ANOGENITAL WARTS ( 9 FDA reports)
ANOPLASTY ( 9 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 9 FDA reports)
AORTIC VALVE CALCIFICATION ( 9 FDA reports)
AORTIC VALVE REPLACEMENT ( 9 FDA reports)
APPETITE DISORDER ( 9 FDA reports)
ARTERIAL STENOSIS ( 9 FDA reports)
ASPERGILLOSIS ( 9 FDA reports)
BACTERIAL SEPSIS ( 9 FDA reports)
BILIARY DILATATION ( 9 FDA reports)
BLADDER HYPERTROPHY ( 9 FDA reports)
BLADDER NECK OPERATION ( 9 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 9 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 9 FDA reports)
BLOOD URIC ACID INCREASED ( 9 FDA reports)
BRAIN CONTUSION ( 9 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 9 FDA reports)
CATHETER REMOVAL ( 9 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 9 FDA reports)
CEREBELLAR INFARCTION ( 9 FDA reports)
CHAPPED LIPS ( 9 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 9 FDA reports)
CLOSTRIDIUM COLITIS ( 9 FDA reports)
COGNITIVE DETERIORATION ( 9 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 9 FDA reports)
CONTRAST MEDIA REACTION ( 9 FDA reports)
CORNEAL OPERATION ( 9 FDA reports)
CREPITATIONS ( 9 FDA reports)
CRYOTHERAPY ( 9 FDA reports)
CULTURE POSITIVE ( 9 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 9 FDA reports)
DEPRESSION SUICIDAL ( 9 FDA reports)
DIABETIC ULCER ( 9 FDA reports)
ENTEROCOLITIS ( 9 FDA reports)
EPIDIDYMITIS ( 9 FDA reports)
FEEDING DISORDER ( 9 FDA reports)
FEMALE STERILISATION ( 9 FDA reports)
FEMORAL ARTERY OCCLUSION ( 9 FDA reports)
FINE MOTOR DELAY ( 9 FDA reports)
FISTULA REPAIR ( 9 FDA reports)
FOOD CRAVING ( 9 FDA reports)
FRACTURE NONUNION ( 9 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 9 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 9 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 9 FDA reports)
HEPATIC NEOPLASM ( 9 FDA reports)
HETEROTAXIA ( 9 FDA reports)
HYPEROSMOLAR STATE ( 9 FDA reports)
HYPERPATHIA ( 9 FDA reports)
HYPOGLYCAEMIC COMA ( 9 FDA reports)
HYPOGONADISM ( 9 FDA reports)
INFUSION SITE INFECTION ( 9 FDA reports)
INJECTION SITE DISCOMFORT ( 9 FDA reports)
INJECTION SITE SCAR ( 9 FDA reports)
INJECTION SITE ULCER ( 9 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 9 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 9 FDA reports)
KIDNEY ENLARGEMENT ( 9 FDA reports)
LIMB OPERATION ( 9 FDA reports)
LYMPHADENITIS ( 9 FDA reports)
MACROGLOSSIA ( 9 FDA reports)
MALABSORPTION ( 9 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 9 FDA reports)
MEDIASTINAL DISORDER ( 9 FDA reports)
METABOLIC SYNDROME ( 9 FDA reports)
METASTASES TO SKIN ( 9 FDA reports)
METATARSALGIA ( 9 FDA reports)
MONONEUROPATHY ( 9 FDA reports)
MUSCLE FATIGUE ( 9 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 9 FDA reports)
NASAL DISCOMFORT ( 9 FDA reports)
NASAL ODOUR ( 9 FDA reports)
NEOPLASM SKIN ( 9 FDA reports)
NEOVASCULARISATION ( 9 FDA reports)
NEUROMYOPATHY ( 9 FDA reports)
OBSESSIVE THOUGHTS ( 9 FDA reports)
OESOPHAGEAL ACHALASIA ( 9 FDA reports)
OPTIC ATROPHY ( 9 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 9 FDA reports)
OROPHARYNGEAL PLAQUE ( 9 FDA reports)
OTOTOXICITY ( 9 FDA reports)
OVERGROWTH BACTERIAL ( 9 FDA reports)
PANCREATIC INSUFFICIENCY ( 9 FDA reports)
PANCREATITIS RELAPSING ( 9 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 9 FDA reports)
PLATELET COUNT ABNORMAL ( 9 FDA reports)
PLEURAL DISORDER ( 9 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 9 FDA reports)
PNEUMONIA VIRAL ( 9 FDA reports)
POLYSUBSTANCE ABUSE ( 9 FDA reports)
PORPHYRIA ( 9 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 9 FDA reports)
PROCEDURAL VOMITING ( 9 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 9 FDA reports)
PULMONARY VASCULAR DISORDER ( 9 FDA reports)
ABDOMINAL INFECTION ( 8 FDA reports)
ABORTION INDUCED ( 8 FDA reports)
ACUTE ABDOMEN ( 8 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 8 FDA reports)
ADRENAL MASS ( 8 FDA reports)
AMAUROSIS FUGAX ( 8 FDA reports)
ANAESTHETIC COMPLICATION ( 8 FDA reports)
ANTIBODY TEST POSITIVE ( 8 FDA reports)
AORTIC ATHEROSCLEROSIS ( 8 FDA reports)
APICECTOMY ( 8 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 8 FDA reports)
ARTERIAL THROMBOSIS ( 8 FDA reports)
ARTERIOVENOUS FISTULA ( 8 FDA reports)
ARTHRITIS INFECTIVE ( 8 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 8 FDA reports)
BENIGN GASTRIC NEOPLASM ( 8 FDA reports)
BILIARY TRACT INFECTION ( 8 FDA reports)
BLADDER DYSFUNCTION ( 8 FDA reports)
BLEEDING TIME PROLONGED ( 8 FDA reports)
BLOOD ALCOHOL INCREASED ( 8 FDA reports)
BLOOD AMYLASE INCREASED ( 8 FDA reports)
BLOOD MAGNESIUM INCREASED ( 8 FDA reports)
BONE GRAFT ( 8 FDA reports)
BRAIN ABSCESS ( 8 FDA reports)
BRAIN MASS ( 8 FDA reports)
BREAST DISCHARGE ( 8 FDA reports)
BREAST OPERATION ( 8 FDA reports)
BULIMIA NERVOSA ( 8 FDA reports)
CAECITIS ( 8 FDA reports)
CALCULUS URINARY ( 8 FDA reports)
CARBON DIOXIDE INCREASED ( 8 FDA reports)
CARDIAC FAILURE ACUTE ( 8 FDA reports)
CARDIAC HYPERTROPHY ( 8 FDA reports)
CARTILAGE ATROPHY ( 8 FDA reports)
CATHETER RELATED INFECTION ( 8 FDA reports)
CHOREOATHETOSIS ( 8 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 8 FDA reports)
CSF PROTEIN INCREASED ( 8 FDA reports)
CUTIS LAXA ( 8 FDA reports)
DEFAECATION URGENCY ( 8 FDA reports)
DELIRIUM TREMENS ( 8 FDA reports)
DERMATITIS ACNEIFORM ( 8 FDA reports)
DYSPRAXIA ( 8 FDA reports)
EAR DISCOMFORT ( 8 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 8 FDA reports)
ERYSIPELAS ( 8 FDA reports)
ETHMOID SINUS SURGERY ( 8 FDA reports)
FACIAL NERVE DISORDER ( 8 FDA reports)
FRACTURED COCCYX ( 8 FDA reports)
GASTRIC BYPASS ( 8 FDA reports)
GASTRIC PH DECREASED ( 8 FDA reports)
GASTROENTERITIS RADIATION ( 8 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 8 FDA reports)
GAZE PALSY ( 8 FDA reports)
GENERAL SYMPTOM ( 8 FDA reports)
GRIEF REACTION ( 8 FDA reports)
H1N1 INFLUENZA ( 8 FDA reports)
HEPATIC ENZYME ABNORMAL ( 8 FDA reports)
HEPATOCELLULAR DAMAGE ( 8 FDA reports)
HEPATORENAL FAILURE ( 8 FDA reports)
HYPERCAPNIA ( 8 FDA reports)
HYPERCORTICOIDISM ( 8 FDA reports)
HYPERPROLACTINAEMIA ( 8 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 8 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 8 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 8 FDA reports)
INCISIONAL HERNIA ( 8 FDA reports)
INJECTION SITE PAPULE ( 8 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 8 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 8 FDA reports)
JOINT STABILISATION ( 8 FDA reports)
LARYNGEAL OEDEMA ( 8 FDA reports)
LENTIGO ( 8 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 8 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 8 FDA reports)
MEDIASTINAL HAEMATOMA ( 8 FDA reports)
MEIBOMIANITIS ( 8 FDA reports)
MENINGISM ( 8 FDA reports)
MENINGITIS ASEPTIC ( 8 FDA reports)
METAMORPHOPSIA ( 8 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 8 FDA reports)
METASTATIC PAIN ( 8 FDA reports)
MONOPARESIS ( 8 FDA reports)
MYOCARDITIS ( 8 FDA reports)
NECROTISING FASCIITIS ( 8 FDA reports)
NEUROMYELITIS OPTICA ( 8 FDA reports)
NEUROSENSORY HYPOACUSIS ( 8 FDA reports)
NEUTROPENIC INFECTION ( 8 FDA reports)
NIGHT BLINDNESS ( 8 FDA reports)
NODAL RHYTHM ( 8 FDA reports)
NONSPECIFIC REACTION ( 8 FDA reports)
NOSOCOMIAL INFECTION ( 8 FDA reports)
OESOPHAGEAL RUPTURE ( 8 FDA reports)
OPEN FRACTURE ( 8 FDA reports)
OPPORTUNISTIC INFECTION ( 8 FDA reports)
OPTIC NERVE DISORDER ( 8 FDA reports)
PERINEURIAL CYST ( 8 FDA reports)
PERITONEAL DIALYSIS ( 8 FDA reports)
PHYSICAL ASSAULT ( 8 FDA reports)
PHYSIOTHERAPY ( 8 FDA reports)
PO2 INCREASED ( 8 FDA reports)
POLYCYTHAEMIA ( 8 FDA reports)
POST THROMBOTIC SYNDROME ( 8 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 8 FDA reports)
PRESCRIBED OVERDOSE ( 8 FDA reports)
PROCEDURAL HYPOTENSION ( 8 FDA reports)
PSEUDOMONAL SEPSIS ( 8 FDA reports)
PSORIATIC ARTHROPATHY ( 8 FDA reports)
RADIATION INJURY ( 8 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 8 FDA reports)
REFLEXES ABNORMAL ( 8 FDA reports)
RENAL INFARCT ( 8 FDA reports)
RENAL OSTEODYSTROPHY ( 8 FDA reports)
SCOTOMA ( 8 FDA reports)
SCROTAL SWELLING ( 8 FDA reports)
SINUS OPERATION ( 8 FDA reports)
SKIN WRINKLING ( 8 FDA reports)
SOMATIC DELUSION ( 8 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 8 FDA reports)
SPINAL PAIN ( 8 FDA reports)
SPLENIC GRANULOMA ( 8 FDA reports)
SPONDYLITIC MYELOPATHY ( 8 FDA reports)
STRIDOR ( 8 FDA reports)
TABLET ISSUE ( 8 FDA reports)
TACHYPHRENIA ( 8 FDA reports)
TESTICULAR PAIN ( 8 FDA reports)
TUBERCULOSIS ( 8 FDA reports)
TUNNEL VISION ( 8 FDA reports)
URINE ABNORMALITY ( 8 FDA reports)
VENOOCCLUSIVE DISEASE ( 8 FDA reports)
VERTEBRAL COLUMN MASS ( 8 FDA reports)
VIRAL LOAD INCREASED ( 8 FDA reports)
VITREOUS HAEMORRHAGE ( 8 FDA reports)
PURPURA SENILE ( 7 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 7 FDA reports)
RED BLOOD CELL ABNORMALITY ( 7 FDA reports)
RENAL ARTERY STENOSIS ( 7 FDA reports)
RENAL ISCHAEMIA ( 7 FDA reports)
RENAL TUBULAR ACIDOSIS ( 7 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 7 FDA reports)
SCROTAL OEDEMA ( 7 FDA reports)
SKIN GRAFT FAILURE ( 7 FDA reports)
SLEEP TERROR ( 7 FDA reports)
SLOW RESPONSE TO STIMULI ( 7 FDA reports)
STEREOTYPY ( 7 FDA reports)
SUFFOCATION FEELING ( 7 FDA reports)
TEETH BRITTLE ( 7 FDA reports)
TERMINAL STATE ( 7 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 7 FDA reports)
THERAPY CESSATION ( 7 FDA reports)
THERAPY REGIMEN CHANGED ( 7 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 7 FDA reports)
TIBIA FRACTURE ( 7 FDA reports)
TONGUE PARALYSIS ( 7 FDA reports)
TONIC CLONIC MOVEMENTS ( 7 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 7 FDA reports)
TOXOPLASMOSIS ( 7 FDA reports)
TRANSPLANT REJECTION ( 7 FDA reports)
TRAUMATIC BRAIN INJURY ( 7 FDA reports)
TROPONIN T INCREASED ( 7 FDA reports)
TUMOUR MARKER INCREASED ( 7 FDA reports)
UTEROVAGINAL PROLAPSE ( 7 FDA reports)
VASCULAR INSUFFICIENCY ( 7 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 7 FDA reports)
VIRAL LABYRINTHITIS ( 7 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
VITH NERVE PARALYSIS ( 7 FDA reports)
VOCAL CORD INFLAMMATION ( 7 FDA reports)
VULVOVAGINAL PRURITUS ( 7 FDA reports)
WOUND DECOMPOSITION ( 7 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 7 FDA reports)
AMENORRHOEA ( 7 FDA reports)
AMPUTATION ( 7 FDA reports)
ANAPHYLACTOID REACTION ( 7 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 7 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 7 FDA reports)
AORTIC DISORDER ( 7 FDA reports)
AORTIC DISSECTION ( 7 FDA reports)
APPLICATION SITE DERMATITIS ( 7 FDA reports)
APPLICATION SITE EXFOLIATION ( 7 FDA reports)
APPLICATION SITE PUSTULES ( 7 FDA reports)
ARTERIAL BYPASS OPERATION ( 7 FDA reports)
ARTERIOSPASM CORONARY ( 7 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 7 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 7 FDA reports)
BLADDER OBSTRUCTION ( 7 FDA reports)
BLOOD CREATININE DECREASED ( 7 FDA reports)
BLOOD PRESSURE ( 7 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 7 FDA reports)
BLOOD UREA ABNORMAL ( 7 FDA reports)
BLOODY DISCHARGE ( 7 FDA reports)
BONE MARROW DISORDER ( 7 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 7 FDA reports)
BRADYARRHYTHMIA ( 7 FDA reports)
CARDIAC OPERATION ( 7 FDA reports)
CATHETER SITE HAEMORRHAGE ( 7 FDA reports)
CATHETERISATION CARDIAC ( 7 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 7 FDA reports)
CIRRHOSIS ALCOHOLIC ( 7 FDA reports)
CONGENITAL ANOMALY ( 7 FDA reports)
CRANIOCEREBRAL INJURY ( 7 FDA reports)
DEVICE ADHESION ISSUE ( 7 FDA reports)
DIPLEGIA ( 7 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 7 FDA reports)
DRUG EFFECT DELAYED ( 7 FDA reports)
DRUG RESISTANCE ( 7 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 7 FDA reports)
DUODENAL STENOSIS ( 7 FDA reports)
DYSLEXIA ( 7 FDA reports)
DYSMORPHISM ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 7 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 7 FDA reports)
ENTEROBACTER SEPSIS ( 7 FDA reports)
EXERCISE LACK OF ( 7 FDA reports)
FACIAL SPASM ( 7 FDA reports)
FEMORAL NECK FRACTURE ( 7 FDA reports)
FOETAL ANTICONVULSANT SYNDROME ( 7 FDA reports)
GASTRITIS HAEMORRHAGIC ( 7 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 7 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 7 FDA reports)
GLOBULINS INCREASED ( 7 FDA reports)
GRANULOCYTE COUNT DECREASED ( 7 FDA reports)
GRANULOMA ( 7 FDA reports)
HAEMANGIOMA OF LIVER ( 7 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 7 FDA reports)
HAEMATOMA INFECTION ( 7 FDA reports)
HEPATIC FIBROSIS ( 7 FDA reports)
HIDRADENITIS ( 7 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 7 FDA reports)
HIV INFECTION ( 7 FDA reports)
HYPERPYREXIA ( 7 FDA reports)
HYPERTENSIVE EMERGENCY ( 7 FDA reports)
HYPOPNOEA ( 7 FDA reports)
HYPOVOLAEMIC SHOCK ( 7 FDA reports)
ILLUSION ( 7 FDA reports)
IMPAIRED SELF-CARE ( 7 FDA reports)
INDUCED LABOUR ( 7 FDA reports)
INFUSION SITE REACTION ( 7 FDA reports)
INJECTION SITE ABSCESS ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 7 FDA reports)
INTESTINAL POLYP ( 7 FDA reports)
IRIS ADHESIONS ( 7 FDA reports)
JOINT ADHESION ( 7 FDA reports)
LEFT VENTRICULAR FAILURE ( 7 FDA reports)
LIP OEDEMA ( 7 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 7 FDA reports)
LYME DISEASE ( 7 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 7 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 7 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 7 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 7 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 7 FDA reports)
NASAL DRYNESS ( 7 FDA reports)
NEPHRECTOMY ( 7 FDA reports)
NERVE BLOCK ( 7 FDA reports)
NEUROMA ( 7 FDA reports)
NEUTROPHILIA ( 7 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 7 FDA reports)
OESOPHAGEAL OPERATION ( 7 FDA reports)
OTITIS MEDIA ACUTE ( 7 FDA reports)
PAIN EXACERBATED ( 7 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 7 FDA reports)
PERFORMANCE STATUS DECREASED ( 7 FDA reports)
PERSECUTORY DELUSION ( 7 FDA reports)
POST POLIO SYNDROME ( 7 FDA reports)
POST PROCEDURAL PAIN ( 7 FDA reports)
PROCEDURAL NAUSEA ( 7 FDA reports)
PROCEDURAL SITE REACTION ( 7 FDA reports)
PROTHROMBIN TIME SHORTENED ( 7 FDA reports)
PULMONARY TOXICITY ( 7 FDA reports)
ABDOMINOPLASTY ( 6 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 6 FDA reports)
ABORTION MISSED ( 6 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 6 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 6 FDA reports)
ALLERGY TO CHEMICALS ( 6 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 6 FDA reports)
ANORECTAL DISORDER ( 6 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 6 FDA reports)
AORTIC OCCLUSION ( 6 FDA reports)
APALLIC SYNDROME ( 6 FDA reports)
APNOEIC ATTACK ( 6 FDA reports)
ASPIRATION PLEURAL CAVITY ( 6 FDA reports)
ATONIC SEIZURES ( 6 FDA reports)
AURICULAR SWELLING ( 6 FDA reports)
AXILLARY PAIN ( 6 FDA reports)
BASAL GANGLION DEGENERATION ( 6 FDA reports)
BASEDOW'S DISEASE ( 6 FDA reports)
BILE DUCT CANCER ( 6 FDA reports)
BILIARY CYST ( 6 FDA reports)
BLOOD ALBUMIN INCREASED ( 6 FDA reports)
BLOOD BICARBONATE INCREASED ( 6 FDA reports)
BLOOD ETHANOL INCREASED ( 6 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 6 FDA reports)
BLOOD URINE ( 6 FDA reports)
BONE CYST ( 6 FDA reports)
BONE FORMATION INCREASED ( 6 FDA reports)
BOWEL SOUNDS ABNORMAL ( 6 FDA reports)
BRAIN CANCER METASTATIC ( 6 FDA reports)
BRAIN DEATH ( 6 FDA reports)
BREAST CANCER STAGE I ( 6 FDA reports)
BREAST ENLARGEMENT ( 6 FDA reports)
BRONCHIAL SECRETION RETENTION ( 6 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 6 FDA reports)
BURNS THIRD DEGREE ( 6 FDA reports)
CANDIDURIA ( 6 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 6 FDA reports)
CARDIAC DEATH ( 6 FDA reports)
CARDIAC OUTPUT DECREASED ( 6 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 6 FDA reports)
CATHETERISATION VENOUS ( 6 FDA reports)
CENTRAL LINE INFECTION ( 6 FDA reports)
CEREBRAL ASPERGILLOSIS ( 6 FDA reports)
CEREBRAL THROMBOSIS ( 6 FDA reports)
CERVICAL MYELOPATHY ( 6 FDA reports)
CHEMOTHERAPY ( 6 FDA reports)
CHONDROCALCINOSIS ( 6 FDA reports)
CHORIORETINAL ATROPHY ( 6 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 6 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 6 FDA reports)
CLONAL EVOLUTION ( 6 FDA reports)
CLONIC CONVULSION ( 6 FDA reports)
COLON CANCER METASTATIC ( 6 FDA reports)
COLORECTAL CANCER ( 6 FDA reports)
COMPARTMENT SYNDROME ( 6 FDA reports)
COMPULSIONS ( 6 FDA reports)
COMPULSIVE SHOPPING ( 6 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 6 FDA reports)
CORNEAL OPACITY ( 6 FDA reports)
CRANIOSYNOSTOSIS ( 6 FDA reports)
CUTANEOUS CONTOUR DEFORMITY ( 6 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 6 FDA reports)
DENTAL IMPLANTATION ( 6 FDA reports)
DIAPHRAGMATIC DISORDER ( 6 FDA reports)
DIARRHOEA INFECTIOUS ( 6 FDA reports)
DISSOCIATIVE DISORDER ( 6 FDA reports)
DIVERTICULAR PERFORATION ( 6 FDA reports)
DRUG LEVEL CHANGED ( 6 FDA reports)
DYSMENORRHOEA ( 6 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 6 FDA reports)
EMBOLISM ARTERIAL ( 6 FDA reports)
ENCEPHALITIS VIRAL ( 6 FDA reports)
ENTEROBACTER INFECTION ( 6 FDA reports)
ENTEROCUTANEOUS FISTULA ( 6 FDA reports)
EOSINOPHILIC PNEUMONIA ( 6 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 6 FDA reports)
ESCHERICHIA BACTERAEMIA ( 6 FDA reports)
EXTREMITY NECROSIS ( 6 FDA reports)
FACIAL NEURALGIA ( 6 FDA reports)
FEELING GUILTY ( 6 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 6 FDA reports)
GALLBLADDER ENLARGEMENT ( 6 FDA reports)
GASTRIC BANDING ( 6 FDA reports)
GASTRIC CANCER ( 6 FDA reports)
GASTRIC ULCER PERFORATION ( 6 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 6 FDA reports)
GASTROINTESTINAL ULCER ( 6 FDA reports)
GRAFT DYSFUNCTION ( 6 FDA reports)
HAEMOLYSIS ( 6 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 6 FDA reports)
HEART SOUNDS ABNORMAL ( 6 FDA reports)
HEPATIC CANCER METASTATIC ( 6 FDA reports)
HEPATITIS VIRAL ( 6 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 6 FDA reports)
HERPES ZOSTER DISSEMINATED ( 6 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 6 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 6 FDA reports)
IMMUNOGLOBULINS INCREASED ( 6 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 6 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 6 FDA reports)
INFUSION SITE ERYTHEMA ( 6 FDA reports)
INJECTION SITE CELLULITIS ( 6 FDA reports)
INTESTINAL FISTULA ( 6 FDA reports)
INTESTINAL INFARCTION ( 6 FDA reports)
INTESTINAL RESECTION ( 6 FDA reports)
INTRACRANIAL ANEURYSM ( 6 FDA reports)
IRON OVERLOAD ( 6 FDA reports)
IVTH NERVE PARALYSIS ( 6 FDA reports)
JOINT CREPITATION ( 6 FDA reports)
JOINT DISLOCATION REDUCTION ( 6 FDA reports)
JOINT INSTABILITY ( 6 FDA reports)
JUGULAR VEIN DISTENSION ( 6 FDA reports)
KLEBSIELLA SEPSIS ( 6 FDA reports)
LABILE HYPERTENSION ( 6 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 6 FDA reports)
LICHEN PLANUS ( 6 FDA reports)
LITHOTRIPSY ( 6 FDA reports)
LIVER ABSCESS ( 6 FDA reports)
LUNG ABSCESS ( 6 FDA reports)
LYMPHATIC OBSTRUCTION ( 6 FDA reports)
MACROCEPHALY ( 6 FDA reports)
MACROCYTOSIS ( 6 FDA reports)
MALIGNANT HYPERTENSION ( 6 FDA reports)
MAMMOPLASTY ( 6 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 6 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 6 FDA reports)
MENINGITIS BACTERIAL ( 6 FDA reports)
MENISCUS REMOVAL ( 6 FDA reports)
METASTASES TO BLADDER ( 6 FDA reports)
MICROALBUMINURIA ( 6 FDA reports)
MOTION SICKNESS ( 6 FDA reports)
MYOSCLEROSIS ( 6 FDA reports)
NECROTISING COLITIS ( 6 FDA reports)
NEOPLASM RECURRENCE ( 6 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 6 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 6 FDA reports)
OESOPHAGEAL CARCINOMA ( 6 FDA reports)
ORCHITIS ( 6 FDA reports)
ORTHOSIS USER ( 6 FDA reports)
ORTHOSTATIC INTOLERANCE ( 6 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 6 FDA reports)
PERINEAL PAIN ( 6 FDA reports)
PERIORBITAL HAEMATOMA ( 6 FDA reports)
PERIORBITAL HAEMORRHAGE ( 6 FDA reports)
PERIRECTAL ABSCESS ( 6 FDA reports)
PERNICIOUS ANAEMIA ( 6 FDA reports)
PLASMAPHERESIS ( 6 FDA reports)
PNEUMONIA KLEBSIELLA ( 6 FDA reports)
POST CONCUSSION SYNDROME ( 6 FDA reports)
POST-TRAUMATIC HEADACHE ( 6 FDA reports)
PREMATURE AGEING ( 6 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 6 FDA reports)
PROSTATECTOMY ( 6 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 6 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 6 FDA reports)
PUPILLARY DISORDER ( 6 FDA reports)
PUSTULAR PSORIASIS ( 6 FDA reports)
QRS AXIS ABNORMAL ( 6 FDA reports)
QUADRIPLEGIA ( 6 FDA reports)
RECTAL CANCER ( 6 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 6 FDA reports)
RENAL ATROPHY ( 6 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 6 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 6 FDA reports)
RHEUMATOID NODULE ( 6 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 6 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 6 FDA reports)
SCLERITIS ( 6 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 6 FDA reports)
SINUS ARREST ( 6 FDA reports)
SKIN DESQUAMATION ( 6 FDA reports)
SKIN OEDEMA ( 6 FDA reports)
SMALL INTESTINE ULCER ( 6 FDA reports)
SOMATISATION DISORDER ( 6 FDA reports)
STERNAL FRACTURE ( 6 FDA reports)
STOMATITIS NECROTISING ( 6 FDA reports)
SUBMANDIBULAR MASS ( 6 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
THROAT LESION ( 6 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 6 FDA reports)
TONIC CONVULSION ( 6 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 6 FDA reports)
TRANCE ( 6 FDA reports)
TROPONIN I INCREASED ( 6 FDA reports)
URAEMIC ENCEPHALOPATHY ( 6 FDA reports)
URETHRAL OBSTRUCTION ( 6 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 6 FDA reports)
URINE KETONE BODY PRESENT ( 6 FDA reports)
UTERINE DISORDER ( 6 FDA reports)
VASCULAR OPERATION ( 6 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 6 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 6 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 6 FDA reports)
VITREOUS DISORDER ( 6 FDA reports)
VOMITING PROJECTILE ( 6 FDA reports)
PYOTHORAX ( 5 FDA reports)
RADIAL NERVE PALSY ( 5 FDA reports)
RASH VESICULAR ( 5 FDA reports)
RECTAL TENESMUS ( 5 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 5 FDA reports)
RENAL COLIC ( 5 FDA reports)
RENAL HAEMORRHAGE ( 5 FDA reports)
RENAL NEOPLASM ( 5 FDA reports)
RETICULOCYTOSIS ( 5 FDA reports)
RETINAL DEGENERATION ( 5 FDA reports)
RETROPERITONEAL HAEMATOMA ( 5 FDA reports)
RHEUMATOID LUNG ( 5 FDA reports)
RIGHT ATRIAL DILATATION ( 5 FDA reports)
ROTAVIRUS TEST POSITIVE ( 5 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 5 FDA reports)
SCROTAL DISORDER ( 5 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 5 FDA reports)
SMALL INTESTINAL STENOSIS ( 5 FDA reports)
STRESS SYMPTOMS ( 5 FDA reports)
SUBCUTANEOUS NODULE ( 5 FDA reports)
SUBDURAL HAEMORRHAGE ( 5 FDA reports)
SUPERINFECTION BACTERIAL ( 5 FDA reports)
SYRINGOMYELIA ( 5 FDA reports)
TEMPORAL ARTERITIS ( 5 FDA reports)
TENDON INJURY ( 5 FDA reports)
TENDON PAIN ( 5 FDA reports)
TENSION HEADACHE ( 5 FDA reports)
TESTICULAR SWELLING ( 5 FDA reports)
THOUGHT BLOCKING ( 5 FDA reports)
THYROID MASS ( 5 FDA reports)
TONGUE BLISTERING ( 5 FDA reports)
TOXIC NODULAR GOITRE ( 5 FDA reports)
TRAUMATIC SHOCK ( 5 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 5 FDA reports)
UHTHOFF'S PHENOMENON ( 5 FDA reports)
ULCERATIVE KERATITIS ( 5 FDA reports)
UMBILICAL CORD ABNORMALITY ( 5 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 5 FDA reports)
URINE FLOW DECREASED ( 5 FDA reports)
UTERINE NEOPLASM ( 5 FDA reports)
VARICELLA ( 5 FDA reports)
VASCULITIS NECROTISING ( 5 FDA reports)
VEIN DISCOLOURATION ( 5 FDA reports)
VOCAL CORD PARESIS ( 5 FDA reports)
VON WILLEBRAND'S DISEASE ( 5 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 5 FDA reports)
WHITE CLOT SYNDROME ( 5 FDA reports)
X-RAY ABNORMAL ( 5 FDA reports)
ABDOMINAL NEOPLASM ( 5 FDA reports)
ABDOMINAL WALL INFECTION ( 5 FDA reports)
ABSCESS INTESTINAL ( 5 FDA reports)
ACCIDENTAL NEEDLE STICK ( 5 FDA reports)
ACHLORHYDRIA ( 5 FDA reports)
ADRENOMEGALY ( 5 FDA reports)
ANAL FISTULA ( 5 FDA reports)
ANAL HAEMORRHAGE ( 5 FDA reports)
ANORECTAL DISCOMFORT ( 5 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 5 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 5 FDA reports)
ASPHYXIA ( 5 FDA reports)
ASTHMATIC CRISIS ( 5 FDA reports)
BACTERIAL DISEASE CARRIER ( 5 FDA reports)
BALLISMUS ( 5 FDA reports)
BENIGN BREAST NEOPLASM ( 5 FDA reports)
BENIGN HEPATIC NEOPLASM ( 5 FDA reports)
BILIARY TRACT DISORDER ( 5 FDA reports)
BIOPSY ( 5 FDA reports)
BLADDER IRRITATION ( 5 FDA reports)
BLADDER NEOPLASM ( 5 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 5 FDA reports)
BLOOD HIV RNA INCREASED ( 5 FDA reports)
BLOOD IRON INCREASED ( 5 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 5 FDA reports)
BLOOD UREA DECREASED ( 5 FDA reports)
BONE MARROW OEDEMA ( 5 FDA reports)
BONE NEOPLASM ( 5 FDA reports)
BONE TRIMMING ( 5 FDA reports)
BRAIN MIDLINE SHIFT ( 5 FDA reports)
BRONCHIAL DISORDER ( 5 FDA reports)
BUNION ( 5 FDA reports)
BURNING MOUTH SYNDROME ( 5 FDA reports)
CALCULUS URETERIC ( 5 FDA reports)
CARDIAC VALVE ABSCESS ( 5 FDA reports)
CAROTID ENDARTERECTOMY ( 5 FDA reports)
CELLULITIS ORBITAL ( 5 FDA reports)
CEREBRAL FUNGAL INFECTION ( 5 FDA reports)
CHEST INJURY ( 5 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 5 FDA reports)
CHONDROPLASTY ( 5 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 5 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 5 FDA reports)
CLEFT LIP ( 5 FDA reports)
CLUBBING ( 5 FDA reports)
COLONIC FISTULA ( 5 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 5 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 5 FDA reports)
CRANIOTOMY ( 5 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 5 FDA reports)
DEAFNESS BILATERAL ( 5 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 5 FDA reports)
DENTAL PLAQUE ( 5 FDA reports)
DEPERSONALISATION ( 5 FDA reports)
DERMATITIS ATOPIC ( 5 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 5 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 5 FDA reports)
DISEASE COMPLICATION ( 5 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 5 FDA reports)
DRUG DETOXIFICATION ( 5 FDA reports)
DRUG TOLERANCE INCREASED ( 5 FDA reports)
DUANE'S SYNDROME ( 5 FDA reports)
DYSCALCULIA ( 5 FDA reports)
DYSTROPHIC CALCIFICATION ( 5 FDA reports)
EFFUSION ( 5 FDA reports)
EPICONDYLITIS ( 5 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 5 FDA reports)
ERECTION INCREASED ( 5 FDA reports)
ERYTHEMA NODOSUM ( 5 FDA reports)
ESSENTIAL TREMOR ( 5 FDA reports)
EXCESSIVE MASTURBATION ( 5 FDA reports)
EYE INFLAMMATION ( 5 FDA reports)
EYELID DISORDER ( 5 FDA reports)
EYELID OPERATION ( 5 FDA reports)
FALLOPIAN TUBE OPERATION ( 5 FDA reports)
FANCONI SYNDROME ( 5 FDA reports)
FEAR OF DISEASE ( 5 FDA reports)
GALLBLADDER PAIN ( 5 FDA reports)
GAMBLING ( 5 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 5 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 5 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 5 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 5 FDA reports)
GLYCOSURIA ( 5 FDA reports)
GOUTY ARTHRITIS ( 5 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 5 FDA reports)
HAEMORRHAGIC DIATHESIS ( 5 FDA reports)
HAIR DISORDER ( 5 FDA reports)
HEART DISEASE CONGENITAL ( 5 FDA reports)
HEAT STROKE ( 5 FDA reports)
HELICOBACTER TEST POSITIVE ( 5 FDA reports)
HEPATIC ARTERY ANEURYSM ( 5 FDA reports)
HEPATIC PAIN ( 5 FDA reports)
HERPES OPHTHALMIC ( 5 FDA reports)
HORNER'S SYNDROME ( 5 FDA reports)
HYPERALBUMINAEMIA ( 5 FDA reports)
HYPERCHLORAEMIA ( 5 FDA reports)
HYPERPLASIA ( 5 FDA reports)
HYPERSEXUALITY ( 5 FDA reports)
HYPERTHERMIA MALIGNANT ( 5 FDA reports)
HYPOPERFUSION ( 5 FDA reports)
HYPOPHYSITIS ( 5 FDA reports)
HYPOTRICHOSIS ( 5 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 5 FDA reports)
IMPETIGO ( 5 FDA reports)
INCISION SITE COMPLICATION ( 5 FDA reports)
INFECTED DERMAL CYST ( 5 FDA reports)
INFECTED SEBACEOUS CYST ( 5 FDA reports)
INFECTIOUS PERITONITIS ( 5 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 5 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 5 FDA reports)
INFLAMMATORY PAIN ( 5 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
INFUSION SITE HAEMORRHAGE ( 5 FDA reports)
INFUSION SITE INFLAMMATION ( 5 FDA reports)
INHALATION THERAPY ( 5 FDA reports)
INJECTION SITE EXFOLIATION ( 5 FDA reports)
INJECTION SITE STINGING ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 5 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 5 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 5 FDA reports)
IRON DEFICIENCY ( 5 FDA reports)
ITCHING SCAR ( 5 FDA reports)
JC VIRUS INFECTION ( 5 FDA reports)
JEALOUS DELUSION ( 5 FDA reports)
JOINT DESTRUCTION ( 5 FDA reports)
KERATOACANTHOMA ( 5 FDA reports)
KIDNEY FIBROSIS ( 5 FDA reports)
LIFE SUPPORT ( 5 FDA reports)
LIGAMENT LAXITY ( 5 FDA reports)
LIP BLISTER ( 5 FDA reports)
LIVER TENDERNESS ( 5 FDA reports)
LIVIDITY ( 5 FDA reports)
LUNG INJURY ( 5 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 5 FDA reports)
MADAROSIS ( 5 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 5 FDA reports)
MEGAKARYOCYTES INCREASED ( 5 FDA reports)
MENOPAUSAL SYMPTOMS ( 5 FDA reports)
METASTASES TO CHEST WALL ( 5 FDA reports)
MORBID THOUGHTS ( 5 FDA reports)
MUSCLE NECROSIS ( 5 FDA reports)
MUSCLE RUPTURE ( 5 FDA reports)
NAIL INFECTION ( 5 FDA reports)
NECK MASS ( 5 FDA reports)
OBSTRUCTION GASTRIC ( 5 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 5 FDA reports)
OPTIC NEUROPATHY ( 5 FDA reports)
ORAL MUCOSA EROSION ( 5 FDA reports)
OROPHARYNGEAL SWELLING ( 5 FDA reports)
OVARIAN ENLARGEMENT ( 5 FDA reports)
PAPULE ( 5 FDA reports)
PARADOXICAL EMBOLISM ( 5 FDA reports)
PARASOMNIA ( 5 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 5 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 5 FDA reports)
PELVIC HAEMATOMA ( 5 FDA reports)
PERICARDIAL HAEMORRHAGE ( 5 FDA reports)
PERIDIVERTICULAR ABSCESS ( 5 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 5 FDA reports)
PNEUMONIA LEGIONELLA ( 5 FDA reports)
POLYMYALGIA RHEUMATICA ( 5 FDA reports)
POLYP COLORECTAL ( 5 FDA reports)
POROCARCINOMA ( 5 FDA reports)
POSTICTAL STATE ( 5 FDA reports)
POSTPARTUM HAEMORRHAGE ( 5 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 5 FDA reports)
PRODUCT COMMINGLING ( 5 FDA reports)
PROTEUS INFECTION ( 5 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 5 FDA reports)
ABDOMINAL WALL ABSCESS ( 4 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 4 FDA reports)
ACUTE LEUKAEMIA ( 4 FDA reports)
ADENOCARCINOMA PANCREAS ( 4 FDA reports)
ALCOHOLIC ( 4 FDA reports)
ALCOHOLIC LIVER DISEASE ( 4 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 4 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 4 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 4 FDA reports)
ANGIOPLASTY ( 4 FDA reports)
ANGIOSARCOMA ( 4 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 4 FDA reports)
ANION GAP DECREASED ( 4 FDA reports)
ANOXIA ( 4 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 4 FDA reports)
AORTIC ANEURYSM RUPTURE ( 4 FDA reports)
AORTIC VALVE STENOSIS ( 4 FDA reports)
APPARENT LIFE THREATENING EVENT ( 4 FDA reports)
APPLICATION SITE SCAR ( 4 FDA reports)
ARTERIAL INSUFFICIENCY ( 4 FDA reports)
BACTERIA STOOL IDENTIFIED ( 4 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 4 FDA reports)
BK VIRUS INFECTION ( 4 FDA reports)
BLADDER CATHETERISATION ( 4 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 4 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 4 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 4 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 4 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 4 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 4 FDA reports)
BLOOD SODIUM ABNORMAL ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 4 FDA reports)
BODY MASS INDEX INCREASED ( 4 FDA reports)
BONE DEFORMITY ( 4 FDA reports)
BONE MARROW DEPRESSION ( 4 FDA reports)
BRADYPNOEA ( 4 FDA reports)
BRAIN DAMAGE ( 4 FDA reports)
BRAIN STEM INFARCTION ( 4 FDA reports)
BREAST DISORDER ( 4 FDA reports)
BREAST HYPERPLASIA ( 4 FDA reports)
BREAST LUMP REMOVAL ( 4 FDA reports)
BRONCHIAL OBSTRUCTION ( 4 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 4 FDA reports)
BUDD-CHIARI SYNDROME ( 4 FDA reports)
CANDIDA SEPSIS ( 4 FDA reports)
CAPSULE PHYSICAL ISSUE ( 4 FDA reports)
CARBON DIOXIDE ABNORMAL ( 4 FDA reports)
CARDIAC ABLATION ( 4 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 4 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 4 FDA reports)
CATARACT DIABETIC ( 4 FDA reports)
CELL DEATH ( 4 FDA reports)
CEREBELLAR HAEMATOMA ( 4 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 4 FDA reports)
CEREBRAL CALCIFICATION ( 4 FDA reports)
CEREBRAL PALSY ( 4 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 4 FDA reports)
CEREBRAL VASOCONSTRICTION ( 4 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 4 FDA reports)
CHANGE OF BOWEL HABIT ( 4 FDA reports)
CHEMICAL BURN OF GASTROINTESTINAL TRACT ( 4 FDA reports)
CHEST WALL PAIN ( 4 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 4 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 4 FDA reports)
CLEFT LIP AND PALATE ( 4 FDA reports)
CLUSTER HEADACHE ( 4 FDA reports)
COLON CANCER STAGE I ( 4 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 4 FDA reports)
COMA SCALE ABNORMAL ( 4 FDA reports)
COMMINUTED FRACTURE ( 4 FDA reports)
CORNEAL DISORDER ( 4 FDA reports)
CRANIAL NERVE DISORDER ( 4 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 4 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 4 FDA reports)
DEVICE DEPOSIT ISSUE ( 4 FDA reports)
DIABETIC BULLOSIS ( 4 FDA reports)
DIABETIC MICROANGIOPATHY ( 4 FDA reports)
DIAPHRAGMATIC HERNIA ( 4 FDA reports)
DISINHIBITION ( 4 FDA reports)
DISLOCATION OF VERTEBRA ( 4 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 4 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 4 FDA reports)
DRESSLER'S SYNDROME ( 4 FDA reports)
DRUG LEVEL FLUCTUATING ( 4 FDA reports)
DRUG THERAPY ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 4 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 4 FDA reports)
DUODENAL ULCER PERFORATION ( 4 FDA reports)
DYSHIDROSIS ( 4 FDA reports)
DYSPAREUNIA ( 4 FDA reports)
ECTOPIC PREGNANCY ( 4 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
EMPTY SELLA SYNDROME ( 4 FDA reports)
ENDARTERECTOMY ( 4 FDA reports)
ENDOCARDIAL FIBROSIS ( 4 FDA reports)
ENDOCARDITIS BACTERIAL ( 4 FDA reports)
ENTEROSTOMY ( 4 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 4 FDA reports)
EPIDERMOLYSIS BULLOSA ( 4 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 4 FDA reports)
EXANTHEM ( 4 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 4 FDA reports)
FABRY'S DISEASE ( 4 FDA reports)
FAT TISSUE INCREASED ( 4 FDA reports)
FEELINGS OF WORTHLESSNESS ( 4 FDA reports)
FOOD ALLERGY ( 4 FDA reports)
FOOD INTERACTION ( 4 FDA reports)
FOOT OPERATION ( 4 FDA reports)
GALACTORRHOEA ( 4 FDA reports)
GALLOP RHYTHM PRESENT ( 4 FDA reports)
GAMMOPATHY ( 4 FDA reports)
GASTRIC DILATATION ( 4 FDA reports)
GASTRIC HYPOMOTILITY ( 4 FDA reports)
GASTRIC PERFORATION ( 4 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 4 FDA reports)
GASTROINTESTINAL NECROSIS ( 4 FDA reports)
GASTROINTESTINAL PERFORATION ( 4 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 4 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 4 FDA reports)
GASTROSTOMY TUBE INSERTION ( 4 FDA reports)
GENERALISED ANXIETY DISORDER ( 4 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 4 FDA reports)
GENITAL RASH ( 4 FDA reports)
GINGIVAL BLISTER ( 4 FDA reports)
GINGIVAL HYPERPLASIA ( 4 FDA reports)
GRAFT COMPLICATION ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HAEMOPHILUS INFECTION ( 4 FDA reports)
HAIR TEXTURE ABNORMAL ( 4 FDA reports)
HALLUCINATION, TACTILE ( 4 FDA reports)
HEART TRANSPLANT REJECTION ( 4 FDA reports)
HEPATIC ADENOMA ( 4 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 4 FDA reports)
HEPATITIS C RNA POSITIVE ( 4 FDA reports)
HEPATITIS E ( 4 FDA reports)
HORMONE LEVEL ABNORMAL ( 4 FDA reports)
HYPERAEMIA ( 4 FDA reports)
HYPOCHONDRIASIS ( 4 FDA reports)
HYPOVITAMINOSIS ( 4 FDA reports)
IIIRD NERVE PARALYSIS ( 4 FDA reports)
IMPATIENCE ( 4 FDA reports)
IMPULSIVE BEHAVIOUR ( 4 FDA reports)
INABILITY TO CRAWL ( 4 FDA reports)
INFANTILE APNOEIC ATTACK ( 4 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 4 FDA reports)
INGUINAL HERNIA REPAIR ( 4 FDA reports)
INJECTION SITE ANAESTHESIA ( 4 FDA reports)
INJECTION SITE DRYNESS ( 4 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 4 FDA reports)
INTERNAL INJURY ( 4 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 4 FDA reports)
INTESTINAL PROLAPSE ( 4 FDA reports)
INTUBATION ( 4 FDA reports)
JOINT WARMTH ( 4 FDA reports)
KERATECTOMY ( 4 FDA reports)
KLEBSIELLA BACTERAEMIA ( 4 FDA reports)
LABYRINTHITIS ( 4 FDA reports)
LACTOBACILLUS INFECTION ( 4 FDA reports)
LAPAROTOMY ( 4 FDA reports)
LEIOMYOSARCOMA ( 4 FDA reports)
LENTICULAR OPACITIES ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LEUKAEMIA PLASMACYTIC ( 4 FDA reports)
LIP ULCERATION ( 4 FDA reports)
LIPIDS INCREASED ( 4 FDA reports)
LIPOPROTEIN (A) INCREASED ( 4 FDA reports)
LISTERIOSIS ( 4 FDA reports)
LIVER TRANSPLANT ( 4 FDA reports)
LONG QT SYNDROME ( 4 FDA reports)
LOSS OF PROPRIOCEPTION ( 4 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 4 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 4 FDA reports)
LUPUS NEPHRITIS ( 4 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 4 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 4 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 4 FDA reports)
MEDIASTINUM NEOPLASM ( 4 FDA reports)
MENINGORRHAGIA ( 4 FDA reports)
MESOTHELIOMA ( 4 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 4 FDA reports)
MICROVASCULAR ANGINA ( 4 FDA reports)
MITRAL VALVE REPLACEMENT ( 4 FDA reports)
MITRAL VALVE STENOSIS ( 4 FDA reports)
MONOCLONAL GAMMOPATHY ( 4 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MONONEUROPATHY MULTIPLEX ( 4 FDA reports)
MUSCLE ABSCESS ( 4 FDA reports)
MYCOSIS FUNGOIDES ( 4 FDA reports)
MYELOFIBROSIS ( 4 FDA reports)
MYOCARDIAL FIBROSIS ( 4 FDA reports)
NAIL BED BLEEDING ( 4 FDA reports)
NEONATAL ASPIRATION ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEURALGIC AMYOTROPHY ( 4 FDA reports)
NEUROGENIC BOWEL ( 4 FDA reports)
NEUROSIS ( 4 FDA reports)
OBESITY SURGERY ( 4 FDA reports)
OCULAR DISCOMFORT ( 4 FDA reports)
OEDEMA GENITAL ( 4 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 4 FDA reports)
ONYCHOMADESIS ( 4 FDA reports)
ORAL FUNGAL INFECTION ( 4 FDA reports)
ORAL MUCOSAL BLISTERING ( 4 FDA reports)
ORAL MUCOSAL ERUPTION ( 4 FDA reports)
ORAL SOFT TISSUE DISORDER ( 4 FDA reports)
ORBITAL OEDEMA ( 4 FDA reports)
ORGANISING PNEUMONIA ( 4 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 4 FDA reports)
PAIN MANAGEMENT ( 4 FDA reports)
PALATAL OEDEMA ( 4 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 4 FDA reports)
PANCREATIC CYST ( 4 FDA reports)
PANCREATIC ENZYMES INCREASED ( 4 FDA reports)
PAPILLARY THYROID CANCER ( 4 FDA reports)
PARADOXICAL DRUG REACTION ( 4 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 4 FDA reports)
PARATHYROID DISORDER ( 4 FDA reports)
PARVOVIRUS INFECTION ( 4 FDA reports)
PELVIC MASS ( 4 FDA reports)
PENILE HAEMORRHAGE ( 4 FDA reports)
PENILE PAIN ( 4 FDA reports)
PENIS DISORDER ( 4 FDA reports)
PERIANAL ABSCESS ( 4 FDA reports)
PERSEVERATION ( 4 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
PHARYNGEAL DISORDER ( 4 FDA reports)
PHIMOSIS ( 4 FDA reports)
PHLEBOTHROMBOSIS ( 4 FDA reports)
PHYSICAL PRODUCT LABEL ISSUE ( 4 FDA reports)
PLACENTAL INSUFFICIENCY ( 4 FDA reports)
PLATELET AGGREGATION INCREASED ( 4 FDA reports)
PLATELET DISORDER ( 4 FDA reports)
PLEOCYTOSIS ( 4 FDA reports)
PLEUROTHOTONUS ( 4 FDA reports)
PNEUMOCOCCAL SEPSIS ( 4 FDA reports)
POLYMEDICATION ( 4 FDA reports)
POLYNEUROPATHY IN MALIGNANT DISEASE ( 4 FDA reports)
POOR DENTAL CONDITION ( 4 FDA reports)
POTENTIATING DRUG INTERACTION ( 4 FDA reports)
PRODUCT FRIABLE ( 4 FDA reports)
PROSTATE INFECTION ( 4 FDA reports)
PROSTATIC ACID PHOSPHATASE INCREASED ( 4 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 4 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 4 FDA reports)
PSEUDOMONAS BRONCHITIS ( 4 FDA reports)
PSYCHOTIC BEHAVIOUR ( 4 FDA reports)
PULMONARY ARTERY STENOSIS ( 4 FDA reports)
PULPITIS DENTAL ( 4 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 4 FDA reports)
PUTAMEN HAEMORRHAGE ( 4 FDA reports)
RADIOTHERAPY TO BRAIN ( 4 FDA reports)
RASH PAPULOSQUAMOUS ( 4 FDA reports)
RECTAL DISCHARGE ( 4 FDA reports)
REFLUX GASTRITIS ( 4 FDA reports)
REGRESSIVE BEHAVIOUR ( 4 FDA reports)
RENAL ABSCESS ( 4 FDA reports)
RENAL CORTICAL NECROSIS ( 4 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 4 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 4 FDA reports)
RETINAL EXUDATES ( 4 FDA reports)
RHYTHM IDIOVENTRICULAR ( 4 FDA reports)
SEBACEOUS CARCINOMA ( 4 FDA reports)
SEBORRHOEA ( 4 FDA reports)
SENILE DEMENTIA ( 4 FDA reports)
SENSORIMOTOR DISORDER ( 4 FDA reports)
SERRATIA INFECTION ( 4 FDA reports)
SERRATIA SEPSIS ( 4 FDA reports)
SIGHT DISABILITY ( 4 FDA reports)
SINOATRIAL BLOCK ( 4 FDA reports)
SKIN EROSION ( 4 FDA reports)
SKIN INFLAMMATION ( 4 FDA reports)
SKIN LESION EXCISION ( 4 FDA reports)
SKIN TOXICITY ( 4 FDA reports)
SKIN TURGOR DECREASED ( 4 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 4 FDA reports)
SLEEP WALKING ( 4 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 4 FDA reports)
SMALL INTESTINAL PERFORATION ( 4 FDA reports)
SOFT TISSUE INFECTION ( 4 FDA reports)
SPASMODIC DYSPHONIA ( 4 FDA reports)
SPIDER VEIN ( 4 FDA reports)
SPINAL CORD HERNIATION ( 4 FDA reports)
SPINAL CORD NEOPLASM ( 4 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 4 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 4 FDA reports)
STRABISMUS ( 4 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 4 FDA reports)
STRESS CARDIOMYOPATHY ( 4 FDA reports)
STRESS INCONTINENCE ( 4 FDA reports)
SUBILEUS ( 4 FDA reports)
SUNBURN ( 4 FDA reports)
SUPERFICIAL INJURY OF EYE ( 4 FDA reports)
SURGICAL PROCEDURE REPEATED ( 4 FDA reports)
SYNCOPE VASOVAGAL ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
TERMINAL INSOMNIA ( 4 FDA reports)
THALAMIC INFARCTION ( 4 FDA reports)
THIRST DECREASED ( 4 FDA reports)
THORACIC OPERATION ( 4 FDA reports)
THYROID OPERATION ( 4 FDA reports)
TOE OPERATION ( 4 FDA reports)
TRACHEAL DISORDER ( 4 FDA reports)
TRANSPLANT FAILURE ( 4 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 4 FDA reports)
TRAUMATIC LUNG INJURY ( 4 FDA reports)
TRICHIASIS ( 4 FDA reports)
TRICHOTILLOMANIA ( 4 FDA reports)
TUMOUR HAEMORRHAGE ( 4 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 4 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 4 FDA reports)
ULNAR TUNNEL SYNDROME ( 4 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 4 FDA reports)
URETERAL STENT INSERTION ( 4 FDA reports)
URETHRAL PAIN ( 4 FDA reports)
URGE INCONTINENCE ( 4 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 4 FDA reports)
URINE OUTPUT INCREASED ( 4 FDA reports)
UTERINE DILATION AND CURETTAGE ( 4 FDA reports)
VAGINAL CANDIDIASIS ( 4 FDA reports)
VAGINITIS BACTERIAL ( 4 FDA reports)
VARICOSE VEIN OPERATION ( 4 FDA reports)
VASCULAR GRAFT ( 4 FDA reports)
VERTEBRAL INJURY ( 4 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
VIRAL LOAD DECREASED ( 4 FDA reports)
VITRECTOMY ( 4 FDA reports)
VULVAL DISORDER ( 4 FDA reports)
VULVAR DYSPLASIA ( 4 FDA reports)
WHIPLASH INJURY ( 4 FDA reports)
XANTHOMA ( 4 FDA reports)
PYOMYOSITIS ( 3 FDA reports)
RADIATION NEUROPATHY ( 3 FDA reports)
RADIATION OESOPHAGITIS ( 3 FDA reports)
RECURRENT CANCER ( 3 FDA reports)
RENAL ADENOMA ( 3 FDA reports)
RENAL HYPERTENSION ( 3 FDA reports)
RESIDUAL URINE VOLUME ( 3 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 3 FDA reports)
RETINAL ISCHAEMIA ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
RICKETTSIOSIS ( 3 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
SALIVARY GLAND MASS ( 3 FDA reports)
SALMONELLA BACTERAEMIA ( 3 FDA reports)
SALMONELLA SEPSIS ( 3 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 3 FDA reports)
SCIATIC NERVE NEUROPATHY ( 3 FDA reports)
SEIZURE LIKE PHENOMENA ( 3 FDA reports)
SENSATION OF BLOCK IN EAR ( 3 FDA reports)
SENSATION OF BLOOD FLOW ( 3 FDA reports)
SEROCONVERSION TEST POSITIVE ( 3 FDA reports)
SHUNT MALFUNCTION ( 3 FDA reports)
SKIN CHAPPED ( 3 FDA reports)
SKIN PAPILLOMA ( 3 FDA reports)
SKULL FRACTURED BASE ( 3 FDA reports)
SMEAR CERVIX ABNORMAL ( 3 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 3 FDA reports)
SOCIAL PHOBIA ( 3 FDA reports)
SOFT TISSUE INJURY ( 3 FDA reports)
SPINAL CORD INFECTION ( 3 FDA reports)
STATUS ASTHMATICUS ( 3 FDA reports)
STATUS MIGRAINOSUS ( 3 FDA reports)
STILLBIRTH ( 3 FDA reports)
STREPTOCOCCAL SEPSIS ( 3 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 3 FDA reports)
SUPRAPUBIC PAIN ( 3 FDA reports)
SYMPTOM MASKED ( 3 FDA reports)
TEMPERATURE DIFFERENCE OF EXTREMITIES ( 3 FDA reports)
TESTIS CANCER ( 3 FDA reports)
THEFT ( 3 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 3 FDA reports)
THREATENED LABOUR ( 3 FDA reports)
THROAT CANCER ( 3 FDA reports)
THROMBOTIC STROKE ( 3 FDA reports)
THYROID PAIN ( 3 FDA reports)
THYROIDECTOMY ( 3 FDA reports)
THYROIDITIS ( 3 FDA reports)
TOE DEFORMITY ( 3 FDA reports)
TONGUE EXFOLIATION ( 3 FDA reports)
TONGUE HAEMORRHAGE ( 3 FDA reports)
TONSILLAR HYPERTROPHY ( 3 FDA reports)
TOOTH DEPOSIT ( 3 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 3 FDA reports)
TRACHEAL STENOSIS ( 3 FDA reports)
TRICHORRHEXIS ( 3 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 3 FDA reports)
TUBERCULIN TEST POSITIVE ( 3 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 3 FDA reports)
ULNAR NERVE INJURY ( 3 FDA reports)
UNEMPLOYMENT ( 3 FDA reports)
UNINTENDED PREGNANCY ( 3 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 3 FDA reports)
UPPER MOTOR NEURONE LESION ( 3 FDA reports)
URETERAL CATHETERISATION ( 3 FDA reports)
URETHRAL MEATUS STENOSIS ( 3 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
URINARY TRACT OBSTRUCTION ( 3 FDA reports)
UTERINE HAEMORRHAGE ( 3 FDA reports)
UTERINE PROLAPSE ( 3 FDA reports)
VAGINAL ABSCESS ( 3 FDA reports)
VAGINAL CANCER ( 3 FDA reports)
VAGINAL FISTULA ( 3 FDA reports)
VAGINITIS ATROPHIC ( 3 FDA reports)
VEIN PAIN ( 3 FDA reports)
VENOUS STASIS ( 3 FDA reports)
VENTRICLE RUPTURE ( 3 FDA reports)
VERY LOW DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
VIRAL MYOCARDITIS ( 3 FDA reports)
VOCAL CORD POLYP ( 3 FDA reports)
VULVAL CANCER ( 3 FDA reports)
VULVOVAGINAL DISCOMFORT ( 3 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 3 FDA reports)
WEGENER'S GRANULOMATOSIS ( 3 FDA reports)
ABDOMINAL OPERATION ( 3 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 3 FDA reports)
ABDOMINAL SYMPTOM ( 3 FDA reports)
ACINETOBACTER BACTERAEMIA ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 3 FDA reports)
ADNEXA UTERI PAIN ( 3 FDA reports)
AGITATION POSTOPERATIVE ( 3 FDA reports)
ALBUMINURIA ( 3 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 3 FDA reports)
ALVEOLITIS ( 3 FDA reports)
ANAL ABSCESS ( 3 FDA reports)
ANGIOGRAM ( 3 FDA reports)
ANKLE OPERATION ( 3 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 3 FDA reports)
ANKYLOSING SPONDYLITIS ( 3 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 3 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 3 FDA reports)
ANTIANDROGEN THERAPY ( 3 FDA reports)
ANTICHOLINERGIC SYNDROME ( 3 FDA reports)
APPLICATION SITE DISCOLOURATION ( 3 FDA reports)
APPLICATION SITE SWELLING ( 3 FDA reports)
APTYALISM ( 3 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 3 FDA reports)
ARTERIAL HAEMORRHAGE ( 3 FDA reports)
ARTERIAL INJURY ( 3 FDA reports)
ARTERIAL STENT INSERTION ( 3 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 3 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 3 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 3 FDA reports)
ASTROCYTOMA ( 3 FDA reports)
AUTONOMIC NEUROPATHY ( 3 FDA reports)
BALLOON ATRIAL SEPTOSTOMY ( 3 FDA reports)
BASAL GANGLIA INFARCTION ( 3 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 3 FDA reports)
BENIGN LUNG NEOPLASM ( 3 FDA reports)
BENIGN NEOPLASM OF SKIN ( 3 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 3 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 3 FDA reports)
BIFASCICULAR BLOCK ( 3 FDA reports)
BILIARY FIBROSIS ( 3 FDA reports)
BIOPSY HEART ( 3 FDA reports)
BIOPSY SKIN ABNORMAL ( 3 FDA reports)
BIPOLAR II DISORDER ( 3 FDA reports)
BLADDER DISCOMFORT ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 3 FDA reports)
BLOOD BILIRUBIN DECREASED ( 3 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 3 FDA reports)
BLOOD OSMOLARITY INCREASED ( 3 FDA reports)
BODY TINEA ( 3 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 3 FDA reports)
BONE SARCOMA ( 3 FDA reports)
BORDERLINE OVARIAN TUMOUR ( 3 FDA reports)
BRAIN COMPRESSION ( 3 FDA reports)
BREAST CANCER STAGE IV ( 3 FDA reports)
BREAST INFLAMMATION ( 3 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 3 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 3 FDA reports)
CALCULUS URETHRAL ( 3 FDA reports)
CARDIAC ASTHMA ( 3 FDA reports)
CARDIAC FIBRILLATION ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
CAROTID INTIMA-MEDIA THICKNESS INCREASED ( 3 FDA reports)
CATHETER SITE CELLULITIS ( 3 FDA reports)
CATHETER SITE DISCHARGE ( 3 FDA reports)
CATHETER SITE ERYTHEMA ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
CAUSTIC INJURY ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 3 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 3 FDA reports)
CEREBROVASCULAR SPASM ( 3 FDA reports)
CHEYNE-STOKES RESPIRATION ( 3 FDA reports)
CHRONIC HEPATITIS ( 3 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 3 FDA reports)
CITROBACTER INFECTION ( 3 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 3 FDA reports)
COCCIDIOIDOMYCOSIS ( 3 FDA reports)
COELIAC ARTERY STENOSIS ( 3 FDA reports)
COGWHEEL RIGIDITY ( 3 FDA reports)
COLECTOMY ( 3 FDA reports)
CONFUSION POSTOPERATIVE ( 3 FDA reports)
CONGENITAL ABSENCE OF CRANIAL VAULT ( 3 FDA reports)
CONGENITAL ANOMALY IN OFFSPRING ( 3 FDA reports)
CONJUNCTIVAL OEDEMA ( 3 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 3 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 3 FDA reports)
CORNEAL SCAR ( 3 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 3 FDA reports)
CORONARY OSTIAL STENOSIS ( 3 FDA reports)
CORRECTIVE LENS USER ( 3 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 3 FDA reports)
DACTYLITIS ( 3 FDA reports)
DARK CIRCLES UNDER EYES ( 3 FDA reports)
DEPENDENCE ON RESPIRATOR ( 3 FDA reports)
DEVICE ISSUE ( 3 FDA reports)
DIABETIC EYE DISEASE ( 3 FDA reports)
DIABETIC FOOT INFECTION ( 3 FDA reports)
DIABETIC GASTROPATHY ( 3 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
DIVORCED ( 3 FDA reports)
DREAMY STATE ( 3 FDA reports)
DRUG INTERACTION POTENTIATION ( 3 FDA reports)
DRUG SCREEN NEGATIVE ( 3 FDA reports)
DRUG TOLERANCE DECREASED ( 3 FDA reports)
DUBIN-JOHNSON SYNDROME ( 3 FDA reports)
DUODENAL SCARRING ( 3 FDA reports)
DUPUYTREN'S CONTRACTURE ( 3 FDA reports)
EAR INJURY ( 3 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 3 FDA reports)
ELECTROLYTE DEPLETION ( 3 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 3 FDA reports)
EMPHYSEMATOUS BULLA ( 3 FDA reports)
ENCEPHALITIC INFECTION ( 3 FDA reports)
ENCOPRESIS ( 3 FDA reports)
ENDOMETRIAL ATROPHY ( 3 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 3 FDA reports)
ENTERITIS INFECTIOUS ( 3 FDA reports)
ENZYME ABNORMALITY ( 3 FDA reports)
EOSINOPHIL COUNT DECREASED ( 3 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 3 FDA reports)
EPIGLOTTITIS ( 3 FDA reports)
EPILEPTIC AURA ( 3 FDA reports)
ESCHAR ( 3 FDA reports)
EXCITABILITY ( 3 FDA reports)
EXPOSURE TO EXTREME TEMPERATURE ( 3 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 3 FDA reports)
EYE INFECTION VIRAL ( 3 FDA reports)
EYE OEDEMA ( 3 FDA reports)
FAECAL VOLUME DECREASED ( 3 FDA reports)
FAT NECROSIS ( 3 FDA reports)
FEBRILE BONE MARROW APLASIA ( 3 FDA reports)
FEELING OF RELAXATION ( 3 FDA reports)
FEMORAL ARTERY ANEURYSM ( 3 FDA reports)
FIBROMATOSIS ( 3 FDA reports)
FISTULA DISCHARGE ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
FUNGAL TEST POSITIVE ( 3 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 3 FDA reports)
GALLBLADDER OEDEMA ( 3 FDA reports)
GASTRIC ULCER HELICOBACTER ( 3 FDA reports)
GASTRIC VARICES ( 3 FDA reports)
GASTRODUODENITIS ( 3 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 3 FDA reports)
GASTROINTESTINAL CARCINOMA ( 3 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 3 FDA reports)
GASTROINTESTINAL INJURY ( 3 FDA reports)
GASTROINTESTINAL MALFORMATION ( 3 FDA reports)
GASTROINTESTINAL OEDEMA ( 3 FDA reports)
GASTROINTESTINAL SURGERY ( 3 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 3 FDA reports)
GENITAL HAEMORRHAGE ( 3 FDA reports)
GENITAL ULCERATION ( 3 FDA reports)
GINGIVITIS ULCERATIVE ( 3 FDA reports)
GRANDIOSITY ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
HAEMATOTOXICITY ( 3 FDA reports)
HAEMOCHROMATOSIS ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 3 FDA reports)
HEMIANOPIA ( 3 FDA reports)
HEMIANOPIA HOMONYMOUS ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 3 FDA reports)
HEPATIC INFECTION ( 3 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 3 FDA reports)
HIGH FREQUENCY ABLATION ( 3 FDA reports)
HYPERSPLENISM ( 3 FDA reports)
HYPERVIGILANCE ( 3 FDA reports)
HYPERVOLAEMIA ( 3 FDA reports)
HYPNOPOMPIC HALLUCINATION ( 3 FDA reports)
IDEAS OF REFERENCE ( 3 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 3 FDA reports)
IMPAIRED FASTING GLUCOSE ( 3 FDA reports)
INADEQUATE DIET ( 3 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 3 FDA reports)
INCREASED BRONCHIAL SECRETION ( 3 FDA reports)
INFECTED CYST ( 3 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 3 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 3 FDA reports)
INFECTIVE THROMBOSIS ( 3 FDA reports)
INFLAMMATORY MARKER INCREASED ( 3 FDA reports)
INFUSION SITE EXTRAVASATION ( 3 FDA reports)
INFUSION SITE MASS ( 3 FDA reports)
INFUSION SITE SWELLING ( 3 FDA reports)
INJECTION SITE DESQUAMATION ( 3 FDA reports)
INJECTION SITE DYSAESTHESIA ( 3 FDA reports)
INJECTION SITE SCAB ( 3 FDA reports)
INTENTION TREMOR ( 3 FDA reports)
INTERNAL HERNIA ( 3 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 3 FDA reports)
ISCHAEMIC NEPHROPATHY ( 3 FDA reports)
JC VIRUS TEST POSITIVE ( 3 FDA reports)
KAPOSI'S SARCOMA ( 3 FDA reports)
LARYNGEAL CANCER ( 3 FDA reports)
LARYNGOSPASM ( 3 FDA reports)
LATEX ALLERGY ( 3 FDA reports)
LAZINESS ( 3 FDA reports)
LDL/HDL RATIO DECREASED ( 3 FDA reports)
LEARNING DISORDER ( 3 FDA reports)
LEUKOPLAKIA ORAL ( 3 FDA reports)
LIBIDO INCREASED ( 3 FDA reports)
LID LAG ( 3 FDA reports)
LIP EXFOLIATION ( 3 FDA reports)
LIPOATROPHY ( 3 FDA reports)
LOOSE STOOLS ( 3 FDA reports)
LOW BIRTH WEIGHT BABY ( 3 FDA reports)
LUNG ADENOCARCINOMA ( 3 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 3 FDA reports)
LYMPH NODE PAIN ( 3 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 3 FDA reports)
MALIGNANT TUMOUR EXCISION ( 3 FDA reports)
MAMMOGRAM ABNORMAL ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 3 FDA reports)
MENINGITIS VIRAL ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
METASTASES TO EYE ( 3 FDA reports)
METASTASES TO MENINGES ( 3 FDA reports)
METASTASES TO OVARY ( 3 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
MITRAL VALVE DISEASE ( 3 FDA reports)
MIXED HYPERLIPIDAEMIA ( 3 FDA reports)
MUCOSAL INFECTION ( 3 FDA reports)
MUSCLE HAEMORRHAGE ( 3 FDA reports)
MYCOBACTERIAL INFECTION ( 3 FDA reports)
NASAL MUCOSAL DISORDER ( 3 FDA reports)
NASOPHARYNGEAL CANCER ( 3 FDA reports)
NEONATAL HYPOXIA ( 3 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 3 FDA reports)
NERVE STIMULATION TEST ABNORMAL ( 3 FDA reports)
NUCHAL RIGIDITY ( 3 FDA reports)
OESOPHAGEAL DISCOMFORT ( 3 FDA reports)
OESOPHAGEAL INFECTION ( 3 FDA reports)
OESOPHAGEAL OEDEMA ( 3 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 3 FDA reports)
OPTIC DISC DISORDER ( 3 FDA reports)
ORAL DISCHARGE ( 3 FDA reports)
ORAL PRURITUS ( 3 FDA reports)
ORAL TORUS ( 3 FDA reports)
OSTEOCHONDROMA ( 3 FDA reports)
OSTEOMALACIA ( 3 FDA reports)
OSTEOMYELITIS ACUTE ( 3 FDA reports)
OVARIAN ADENOMA ( 3 FDA reports)
OVARIAN CANCER RECURRENT ( 3 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 3 FDA reports)
PAIN THRESHOLD DECREASED ( 3 FDA reports)
PAINFUL DEFAECATION ( 3 FDA reports)
PANCREATIC MASS ( 3 FDA reports)
PANNICULITIS ( 3 FDA reports)
PANNICULITIS LOBULAR ( 3 FDA reports)
PARACENTESIS ( 3 FDA reports)
PARAKERATOSIS ( 3 FDA reports)
PARALYSIS FLACCID ( 3 FDA reports)
PARASITE BLOOD TEST POSITIVE ( 3 FDA reports)
PARATHYROIDECTOMY ( 3 FDA reports)
PAROTID GLAND INFLAMMATION ( 3 FDA reports)
PAROTITIS ( 3 FDA reports)
PERICARDIAL FIBROSIS ( 3 FDA reports)
PERICARDITIS CONSTRICTIVE ( 3 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 3 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 3 FDA reports)
PERITONEAL DISORDER ( 3 FDA reports)
PERITONEAL HAEMORRHAGE ( 3 FDA reports)
PHLEBITIS INFECTIVE ( 3 FDA reports)
PHLEBITIS SUPERFICIAL ( 3 FDA reports)
PHONOPHOBIA ( 3 FDA reports)
PHYSICAL ABUSE ( 3 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 3 FDA reports)
PIGMENTATION BUCCAL ( 3 FDA reports)
PITUITARY TUMOUR ( 3 FDA reports)
PLEURAL CALCIFICATION ( 3 FDA reports)
PNEUMONIA MYCOPLASMAL ( 3 FDA reports)
POLYMYOSITIS ( 3 FDA reports)
PORPHYRIA ACUTE ( 3 FDA reports)
POST PROCEDURAL BILE LEAK ( 3 FDA reports)
POST PROCEDURAL DIARRHOEA ( 3 FDA reports)
POST-TRAUMATIC PAIN ( 3 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 3 FDA reports)
PREMENSTRUAL SYNDROME ( 3 FDA reports)
PREVENTIVE SURGERY ( 3 FDA reports)
PRODUCT COATING ISSUE ( 3 FDA reports)
PRODUCT SIZE ISSUE ( 3 FDA reports)
PROPHYLAXIS OF NAUSEA AND VOMITING ( 3 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 3 FDA reports)
PTERYGIUM ( 3 FDA reports)
PUBIS FRACTURE ( 3 FDA reports)
PULMONARY ARTERY DILATATION ( 3 FDA reports)
PULMONARY CALCIFICATION ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
PULMONARY VALVE STENOSIS ( 3 FDA reports)
ABDOMINAL HAEMATOMA ( 2 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 2 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 2 FDA reports)
ABNORMAL WEIGHT GAIN ( 2 FDA reports)
ACCIDENTAL POISONING ( 2 FDA reports)
ACINETOBACTER TEST POSITIVE ( 2 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 2 FDA reports)
ACQUIRED PORPHYRIA ( 2 FDA reports)
ACROMEGALY ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACTIVATION SYNDROME ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 2 FDA reports)
ADENOTONSILLECTOMY ( 2 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 2 FDA reports)
ADRENAL ATROPHY ( 2 FDA reports)
ADRENALECTOMY ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
AIDS ENCEPHALOPATHY ( 2 FDA reports)
AIR EMBOLISM ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALCOHOL PROBLEM ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ALPHA 2 GLOBULIN DECREASED ( 2 FDA reports)
AMINOACIDURIA ( 2 FDA reports)
AMMONIA ( 2 FDA reports)
AMPHETAMINES POSITIVE ( 2 FDA reports)
AMYLASE INCREASED ( 2 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
ANEURYSM RUPTURED ( 2 FDA reports)
ANEURYSMAL BONE CYST ( 2 FDA reports)
ANORECTAL ULCER ( 2 FDA reports)
ANTEROGRADE AMNESIA ( 2 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
APPENDIX DISORDER ( 2 FDA reports)
APPLICATION SITE CELLULITIS ( 2 FDA reports)
APPLICATION SITE EROSION ( 2 FDA reports)
ARACHNOIDITIS ( 2 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 2 FDA reports)
ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
ARTHRODESIS ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 2 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 2 FDA reports)
AUTOMATIC BLADDER ( 2 FDA reports)
AVULSION FRACTURE ( 2 FDA reports)
AXILLARY MASS ( 2 FDA reports)
AXILLARY VEIN THROMBOSIS ( 2 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 2 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BALANITIS ( 2 FDA reports)
BAND SENSATION ( 2 FDA reports)
BARIUM SWALLOW ABNORMAL ( 2 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 2 FDA reports)
BASAL GANGLIA STROKE ( 2 FDA reports)
BASILAR MIGRAINE ( 2 FDA reports)
BEREAVEMENT REACTION ( 2 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 2 FDA reports)
BIOPSY LYMPH GLAND ( 2 FDA reports)
BLADDER CANCER RECURRENT ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLADDER MASS ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 2 FDA reports)
BLOOD AMYLASE DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD CARBON MONOXIDE INCREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD CREATINE DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 2 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE ABNORMAL ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 2 FDA reports)
BLOOD OESTROGEN DECREASED ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BODY HEIGHT INCREASED ( 2 FDA reports)
BONE METABOLISM DISORDER ( 2 FDA reports)
BOWEN'S DISEASE ( 2 FDA reports)
BRAIN STEM SYNDROME ( 2 FDA reports)
BREAST CALCIFICATIONS ( 2 FDA reports)
BREAST CANCER IN SITU ( 2 FDA reports)
BREAST CANCER STAGE II ( 2 FDA reports)
BREECH PRESENTATION ( 2 FDA reports)
BRONCHIAL IRRITATION ( 2 FDA reports)
BRONCHITIS VIRAL ( 2 FDA reports)
BRONCHOPLEURAL FISTULA ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
BURKITT'S LYMPHOMA ( 2 FDA reports)
BURNOUT SYNDROME ( 2 FDA reports)
CANCER IN REMISSION ( 2 FDA reports)
CARBUNCLE ( 2 FDA reports)
CARDIAC DISCOMFORT ( 2 FDA reports)
CARDIAC ENZYMES ( 2 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 2 FDA reports)
CARDIAC PERFORATION ( 2 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 2 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 2 FDA reports)
CARDIAC VALVE VEGETATION ( 2 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 2 FDA reports)
CARTILAGE GRAFT ( 2 FDA reports)
CAST APPLICATION ( 2 FDA reports)
CATAPLEXY ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 2 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 2 FDA reports)
CEREBELLAR ATROPHY ( 2 FDA reports)
CEREBELLAR ISCHAEMIA ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL HYPOPERFUSION ( 2 FDA reports)
CERVICAL CYST ( 2 FDA reports)
CERVIX CARCINOMA RECURRENT ( 2 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 2 FDA reports)
CERVIX CARCINOMA STAGE III ( 2 FDA reports)
CERVIX CARCINOMA STAGE IV ( 2 FDA reports)
CHEMICAL EYE INJURY ( 2 FDA reports)
CHILLBLAINS ( 2 FDA reports)
CHOLESTASIS OF PREGNANCY ( 2 FDA reports)
CHOROIDAL EFFUSION ( 2 FDA reports)
CHROMOSOMAL DELETION ( 2 FDA reports)
CHRONIC FATIGUE SYNDROME ( 2 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
CITROBACTER TEST POSITIVE ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 2 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 2 FDA reports)
COAGULATION TEST ABNORMAL ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COMPLICATION OF PREGNANCY ( 2 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 2 FDA reports)
CONFABULATION ( 2 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 2 FDA reports)
CONGENITAL SPINAL CORD ANOMALY ( 2 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 2 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
CORONARY ARTERY DISSECTION ( 2 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 2 FDA reports)
CRANIAL NERVE PARALYSIS ( 2 FDA reports)
CREATINE URINE INCREASED ( 2 FDA reports)
CREATININE URINE INCREASED ( 2 FDA reports)
CRUSH SYNDROME ( 2 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 2 FDA reports)
CSF NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
CSF PRESSURE INCREASED ( 2 FDA reports)
CSF PROTEIN ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CYANOSIS CENTRAL ( 2 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 2 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 2 FDA reports)
DEATH OF RELATIVE ( 2 FDA reports)
DEJA VU ( 2 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 2 FDA reports)
DENERVATION ATROPHY ( 2 FDA reports)
DENGUE FEVER ( 2 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 2 FDA reports)
DENTAL TREATMENT ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DERMATILLOMANIA ( 2 FDA reports)
DERMATOMYOSITIS ( 2 FDA reports)
DEVICE COMPONENT ISSUE ( 2 FDA reports)
DEVICE DAMAGE ( 2 FDA reports)
DEVICE DISLOCATION ( 2 FDA reports)
DIABETIC GANGRENE ( 2 FDA reports)
DIARRHOEA NEONATAL ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DISACCHARIDE METABOLISM DISORDER ( 2 FDA reports)
DISBACTERIOSIS ( 2 FDA reports)
DISTAL INTESTINAL OBSTRUCTION SYNDROME ( 2 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 2 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 2 FDA reports)
DRUG ADDICT ( 2 FDA reports)
DRUG DIVERSION ( 2 FDA reports)
DRUG EFFECT PROLONGED ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
EAR INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
EAR PRURITUS ( 2 FDA reports)
EARLY MORNING AWAKENING ( 2 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
EJACULATION DELAYED ( 2 FDA reports)
EJACULATION DISORDER ( 2 FDA reports)
EJECTION FRACTION ABNORMAL ( 2 FDA reports)
ELECTRIC SHOCK ( 2 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 2 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 2 FDA reports)
EMBOLIA CUTIS MEDICAMENTOSA ( 2 FDA reports)
EMBOLISM INFECTIVE ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENDOCRINE PANCREATIC DISORDER ( 2 FDA reports)
ENDOMETRIAL SARCOMA ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
EOSINOPHILS URINE PRESENT ( 2 FDA reports)
EPHELIDES ( 2 FDA reports)
EPIDERMAL NAEVUS ( 2 FDA reports)
EPIDURAL ANAESTHESIA ( 2 FDA reports)
EPISCLERITIS ( 2 FDA reports)
ERYTHEMA ANNULARE ( 2 FDA reports)
EUTHANASIA ( 2 FDA reports)
EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
EXTERNAL EAR PAIN ( 2 FDA reports)
EXTRASKELETAL OSTEOSARCOMA ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
FACIAL ASYMMETRY ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 2 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
FEAR OF FALLING ( 2 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 2 FDA reports)
FEEDING DISORDER NEONATAL ( 2 FDA reports)
FEEDING TUBE COMPLICATION ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FLASHBACK ( 2 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 2 FDA reports)
FLUID IMBALANCE ( 2 FDA reports)
FLUOROSIS ( 2 FDA reports)
FOOD AVERSION ( 2 FDA reports)
FOREIGN BODY IN EYE ( 2 FDA reports)
FULL BLOOD COUNT INCREASED ( 2 FDA reports)
FUMBLING ( 2 FDA reports)
FUNCTIONAL RESIDUAL CAPACITY DECREASED ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
FUNGAL CYSTITIS ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
FUNGAL PERITONITIS ( 2 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GASTRIC CYST ( 2 FDA reports)
GASTROENTERITIS NOROVIRUS ( 2 FDA reports)
GASTROENTERITIS SALMONELLA ( 2 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 2 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
GENITAL DISCHARGE ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GLOBAL AMNESIA ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE IV ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
HAEMORRHAGIC ASCITES ( 2 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HALO VISION ( 2 FDA reports)
HEAD AND NECK CANCER ( 2 FDA reports)
HEART VALVE REPLACEMENT ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HEAVY EXPOSURE TO ULTRAVIOLET LIGHT ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEPATIC INFECTION FUNGAL ( 2 FDA reports)
HEPATIC ISCHAEMIA ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT NON-RESECTABLE ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS B CORE ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS C VIRUS ( 2 FDA reports)
HEPATITIS GRANULOMATOUS ( 2 FDA reports)
HEREDITARY ANGIOEDEMA ( 2 FDA reports)
HERPES OESOPHAGITIS ( 2 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 2 FDA reports)
HERPES ZOSTER INFECTION NEUROLOGICAL ( 2 FDA reports)
HIGH TURNOVER OSTEOPATHY ( 2 FDA reports)
HIP SWELLING ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HOMELESS ( 2 FDA reports)
HYDROURETER ( 2 FDA reports)
HYPERCREATINAEMIA ( 2 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 2 FDA reports)
HYPERKINESIA ( 2 FDA reports)
HYPERMAGNESAEMIA ( 2 FDA reports)
HYPERPROTEINAEMIA ( 2 FDA reports)
HYPERTELORISM OF ORBIT ( 2 FDA reports)
HYPERTONIA NEONATAL ( 2 FDA reports)
HYPERVISCOSITY SYNDROME ( 2 FDA reports)
HYPOAESTHESIA EYE ( 2 FDA reports)
HYPOPROTHROMBINAEMIA ( 2 FDA reports)
HYPOURICAEMIA ( 2 FDA reports)
IGA NEPHROPATHY ( 2 FDA reports)
IIIRD NERVE PARESIS ( 2 FDA reports)
ILEAL PERFORATION ( 2 FDA reports)
ILEOSTOMY ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 2 FDA reports)
IMPLANT SITE PAIN ( 2 FDA reports)
IMPLANT SITE REACTION ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INFECTED BITES ( 2 FDA reports)
INFERTILITY ( 2 FDA reports)
INFERTILITY MALE ( 2 FDA reports)
INFUSION SITE PHLEBITIS ( 2 FDA reports)
INHIBITORY DRUG INTERACTION ( 2 FDA reports)
INJECTION SITE FIBROSIS ( 2 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 2 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 2 FDA reports)
INTERTRIGO CANDIDA ( 2 FDA reports)
INTERVERTEBRAL DISC INJURY ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
INTESTINAL VARICES ( 2 FDA reports)
INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
IRIS CYST ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
JOINT DISLOCATION PATHOLOGICAL ( 2 FDA reports)
KELOID SCAR ( 2 FDA reports)
KUSSMAUL RESPIRATION ( 2 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LACRIMAL DISORDER ( 2 FDA reports)
LACRIMATION DECREASED ( 2 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LEGIONELLA INFECTION ( 2 FDA reports)
LEUCINE AMINOPEPTIDASE INCREASED ( 2 FDA reports)
LEUKAEMIA RECURRENT ( 2 FDA reports)
LEUKAEMOID REACTION ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIMB REDUCTION DEFECT ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 2 FDA reports)
LIVER GRAFT LOSS ( 2 FDA reports)
LIVER SCAN ABNORMAL ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
LOCKED-IN SYNDROME ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LOSS OF VISUAL CONTRAST SENSITIVITY ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LOW TURNOVER OSTEOPATHY ( 2 FDA reports)
LUMBAR HERNIA ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE I ( 2 FDA reports)
LUNG TRANSPLANT ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LYMPH NODES SCAN ABNORMAL ( 2 FDA reports)
LYMPHADENECTOMY ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
LYMPHORRHOEA ( 2 FDA reports)
MACULAR CYST ( 2 FDA reports)
MACULAR PIGMENTATION ( 2 FDA reports)
MACULAR REFLEX ABNORMAL ( 2 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 2 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 2 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 2 FDA reports)
MANTLE CELL LYMPHOMA RECURRENT ( 2 FDA reports)
MARASMUS ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MEAN CELL VOLUME DECREASED ( 2 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 2 FDA reports)
MEDICAL DIET ( 2 FDA reports)
MELANOSIS ( 2 FDA reports)
MELAS SYNDROME ( 2 FDA reports)
MENINGITIS CHEMICAL ( 2 FDA reports)
MENOMETRORRHAGIA ( 2 FDA reports)
MENSTRUATION DELAYED ( 2 FDA reports)
MESENTERIC PANNICULITIS ( 2 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 2 FDA reports)
METASTASES TO GALLBLADDER ( 2 FDA reports)
METASTASES TO PANCREAS ( 2 FDA reports)
METASTASES TO PELVIS ( 2 FDA reports)
METASTASES TO SPLEEN ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 2 FDA reports)
MITRAL VALVE REPAIR ( 2 FDA reports)
MIXED DEAFNESS ( 2 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 2 FDA reports)
MUCOSAL DISCOLOURATION ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 2 FDA reports)
MUSCLE FIBROSIS ( 2 FDA reports)
MYOPATHY TOXIC ( 2 FDA reports)
MYOSITIS OSSIFICANS ( 2 FDA reports)
NASAL ULCER ( 2 FDA reports)
NEEDLE ISSUE ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NEONATAL TACHYPNOEA ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NERVE ROOT INJURY ( 2 FDA reports)
NEUROLOGICAL INFECTION ( 2 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NO ADVERSE REACTION ( 2 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NODAL ARRHYTHMIA ( 2 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 2 FDA reports)
NONINFECTIOUS PERITONITIS ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 2 FDA reports)
OLIGOMENORRHOEA ( 2 FDA reports)
ONCOLOGIC COMPLICATION ( 2 FDA reports)
ONYCHOPHAGIA ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OPISTHOTONUS ( 2 FDA reports)
OPTIC NERVE INJURY ( 2 FDA reports)
OPTIC NERVE NEOPLASM ( 2 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 2 FDA reports)
ORGASM ABNORMAL ( 2 FDA reports)
ORTHOPEDIC PROCEDURE ( 2 FDA reports)
OSCILLOPSIA ( 2 FDA reports)
OSTEOGENESIS IMPERFECTA ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
OVARIAN CANCER METASTATIC ( 2 FDA reports)
OVARIAN NEOPLASM ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 2 FDA reports)
PANCREAS TRANSPLANT ( 2 FDA reports)
PANCREATIC ATROPHY ( 2 FDA reports)
PANCREATICODUODENECTOMY ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PARADOXICAL PAIN ( 2 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 2 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 2 FDA reports)
PASSIVE SMOKING ( 2 FDA reports)
PEDAL PULSE DECREASED ( 2 FDA reports)
PELVIC DISCOMFORT ( 2 FDA reports)
PERFORATION BILE DUCT ( 2 FDA reports)
PERICORONITIS ( 2 FDA reports)
PERINEPHRIC COLLECTION ( 2 FDA reports)
PERIODONTAL INFECTION ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 2 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 2 FDA reports)
PHAEOCHROMOCYTOMA ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHOTOCOAGULATION ( 2 FDA reports)
PHOTODERMATOSIS ( 2 FDA reports)
PILONIDAL CYST ( 2 FDA reports)
PIRIFORMIS SYNDROME ( 2 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 2 FDA reports)
PLANTAR ERYTHEMA ( 2 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 2 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PNEUMONIA HERPES VIRAL ( 2 FDA reports)
PNEUMONITIS CHEMICAL ( 2 FDA reports)
POLYCYSTIC OVARIES ( 2 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 2 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 2 FDA reports)
PORPHYRINS URINE INCREASED ( 2 FDA reports)
PORTOPULMONARY HYPERTENSION ( 2 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 2 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 2 FDA reports)
POST PROCEDURAL DRAINAGE ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 2 FDA reports)
POST PROCEDURAL STROKE ( 2 FDA reports)
POST PROCEDURAL SWELLING ( 2 FDA reports)
POSTOPERATIVE ADHESION ( 2 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 2 FDA reports)
POSTURING ( 2 FDA reports)
PRECANCEROUS SKIN LESION ( 2 FDA reports)
PRIMARY PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
PROCEDURAL HYPERTENSION ( 2 FDA reports)
PRODUCT CONTAMINATION ( 2 FDA reports)
PRODUCT LABEL ISSUE ( 2 FDA reports)
PRODUCT PACKAGING ISSUE ( 2 FDA reports)
PRODUCT TAMPERING ( 2 FDA reports)
PROSTHESIS IMPLANTATION ( 2 FDA reports)
PROTEIN S DEFICIENCY ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PSEUDOBULBAR PALSY ( 2 FDA reports)
PSEUDODEMENTIA ( 2 FDA reports)
PSEUDOLYMPHOMA ( 2 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 2 FDA reports)
PSEUDOPORPHYRIA ( 2 FDA reports)
PSYCHIATRIC EVALUATION ( 2 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
PUBIC RAMI FRACTURE ( 2 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY NECROSIS ( 2 FDA reports)
PULMONARY SARCOIDOSIS ( 2 FDA reports)
PUPILLARY DEFORMITY ( 2 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 2 FDA reports)
PUS IN STOOL ( 2 FDA reports)
PYELONEPHRITIS CHRONIC ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 2 FDA reports)
RADIATION PNEUMONITIS ( 2 FDA reports)
RADICULAR SYNDROME ( 2 FDA reports)
RAPID CORRECTION OF HYPONATRAEMIA ( 2 FDA reports)
RASH SCARLATINIFORM ( 2 FDA reports)
REACTION TO AZO-DYES ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 2 FDA reports)
RECTAL PERFORATION ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 2 FDA reports)
RED MAN SYNDROME ( 2 FDA reports)
REFRACTORY ANAEMIA ( 2 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 2 FDA reports)
RENAL APLASIA ( 2 FDA reports)
RENAL CANCER METASTATIC ( 2 FDA reports)
RENAL SCAN ABNORMAL ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 2 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETINAL ARTERY OCCLUSION ( 2 FDA reports)
RETINAL INJURY ( 2 FDA reports)
RETINAL OEDEMA ( 2 FDA reports)
RETINAL OPERATION ( 2 FDA reports)
RETINAL TOXICITY ( 2 FDA reports)
RETINAL VASCULAR OCCLUSION ( 2 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 2 FDA reports)
RETROGRADE AMNESIA ( 2 FDA reports)
RETROPERITONEAL NEOPLASM METASTATIC ( 2 FDA reports)
RHINOVIRUS INFECTION ( 2 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 2 FDA reports)
ROTAVIRUS INFECTION ( 2 FDA reports)
SACCADIC EYE MOVEMENT ( 2 FDA reports)
SCHIZOTYPAL PERSONALITY DISORDER ( 2 FDA reports)
SCLERODERMA RENAL CRISIS ( 2 FDA reports)
SCROTAL HAEMATOCOELE ( 2 FDA reports)
SELF MUTILATION ( 2 FDA reports)
SENSORY GANGLIONITIS ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SEPTIC ENCEPHALOPATHY ( 2 FDA reports)
SEPTOPLASTY ( 2 FDA reports)
SERONEGATIVE ARTHRITIS ( 2 FDA reports)
SERRATIA TEST POSITIVE ( 2 FDA reports)
SERUM FERRITIN ABNORMAL ( 2 FDA reports)
SERUM FERRITIN DECREASED ( 2 FDA reports)
SEX HORMONE BINDING GLOBULIN DECREASED ( 2 FDA reports)
SEXUAL ASSAULT VICTIM ( 2 FDA reports)
SHOCK HYPOGLYCAEMIC ( 2 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 2 FDA reports)
SINUS PERFORATION ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN DISCOMFORT ( 2 FDA reports)
SKIN FRAGILITY ( 2 FDA reports)
SKIN SENSITISATION ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SMOKER ( 2 FDA reports)
SOFT TISSUE INFLAMMATION ( 2 FDA reports)
SPINA BIFIDA ( 2 FDA reports)
SPINAL CLAUDICATION ( 2 FDA reports)
SPINAL CORD INFARCTION ( 2 FDA reports)
SPINAL CORD INJURY CERVICAL ( 2 FDA reports)
SPINAL CORD OPERATION ( 2 FDA reports)
SPINAL EPIDURAL HAEMORRHAGE ( 2 FDA reports)
SPINAL HAEMATOMA ( 2 FDA reports)
SPLEEN SCAN ABNORMAL ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STOOL ANALYSIS ABNORMAL ( 2 FDA reports)
STREPTOCOCCAL ABSCESS ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUBSTANCE ABUSER ( 2 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
SURGICAL STAPLING ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 2 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 2 FDA reports)
TACHYCARDIA PAROXYSMAL ( 2 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 2 FDA reports)
TEMPORAL LOBE EPILEPSY ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
THORACIC CAVITY DRAINAGE ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THYROID ATROPHY ( 2 FDA reports)
THYROTOXIC CRISIS ( 2 FDA reports)
TINEA CRURIS ( 2 FDA reports)
TONGUE COATED ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TRACHEAL OBSTRUCTION ( 2 FDA reports)
TRACHEITIS ( 2 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 2 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 2 FDA reports)
TRANSPLANT ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
TRAUMATIC HAEMORRHAGE ( 2 FDA reports)
TRICHOMONIASIS ( 2 FDA reports)
TRICUSPID VALVE REPLACEMENT ( 2 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 2 FDA reports)
TUMOUR FLARE ( 2 FDA reports)
TYMPANOSCLEROSIS ( 2 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 2 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
UNDERWEIGHT ( 2 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 2 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
URETHRAL ATROPHY ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URINARY TRACT INFLAMMATION ( 2 FDA reports)
UROGENITAL ATROPHY ( 2 FDA reports)
UROGENITAL TRICHOMONIASIS ( 2 FDA reports)
URTICARIA GENERALISED ( 2 FDA reports)
UTERINE SPASM ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VAGINAL CYST ( 2 FDA reports)
VAGINAL DISORDER ( 2 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VAGINAL OPERATION ( 2 FDA reports)
VAGUS NERVE DISORDER ( 2 FDA reports)
VARICOSE ULCERATION ( 2 FDA reports)
VASCULAR BYPASS GRAFT ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VENA CAVA FILTER INSERTION ( 2 FDA reports)
VENOUS PRESSURE JUGULAR ( 2 FDA reports)
VISUAL BRIGHTNESS ( 2 FDA reports)
VISUAL PATHWAY DISORDER ( 2 FDA reports)
VITAMIN D ABNORMAL ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
VULVAL OEDEMA ( 2 FDA reports)
VULVOVAGINAL PAIN ( 2 FDA reports)
WALKING DISTANCE TEST ABNORMAL ( 2 FDA reports)
WEANING FAILURE ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
WOUND ABSCESS ( 2 FDA reports)
YERSINIA INFECTION ( 2 FDA reports)
PYELONEPHRITIS FUNGAL ( 1 FDA reports)
PYROGLUTAMATE INCREASED ( 1 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
RADIATION SICKNESS SYNDROME ( 1 FDA reports)
RADICAL MASTECTOMY ( 1 FDA reports)
RADICULITIS BRACHIAL ( 1 FDA reports)
RADICULITIS CERVICAL ( 1 FDA reports)
RADICULOTOMY ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
REBOUND HYPERTENSION ( 1 FDA reports)
RECTAL PROLAPSE REPAIR ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
RELAPSING POLYCHONDRITIS ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESPIRATORY DEPTH INCREASED ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETICULOCYTOPENIA ( 1 FDA reports)
RETINAL ARTERY STENOSIS ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETINITIS PIGMENTOSA ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RHINOLARYNGITIS ( 1 FDA reports)
RIGHT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
ROSEOLOVIRUS TEST POSITIVE ( 1 FDA reports)
ROUTINE HEALTH MAINTENANCE ( 1 FDA reports)
ROUX LOOP CONVERSION ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SALIVARY GLAND NEOPLASM ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCROTAL ABSCESS ( 1 FDA reports)
SCROTAL CANCER ( 1 FDA reports)
SCROTAL VARICOSE VEINS ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SEMINOMA ( 1 FDA reports)
SENSATION OF PRESSURE IN EAR ( 1 FDA reports)
SEROLOGY ABNORMAL ( 1 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHOULDER ARTHROPLASTY ( 1 FDA reports)
SHUNT INFECTION ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN CANCER METASTATIC ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKULL X-RAY ABNORMAL ( 1 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SMALL INTESTINE GANGRENE ( 1 FDA reports)
SMALL INTESTINE OPERATION ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SPECIFIC GRAVITY URINE DECREASED ( 1 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPINOCEREBELLAR DISORDER ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENIC VARICES ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPLENORENAL SHUNT ( 1 FDA reports)
SPONDYLOARTHROPATHY ( 1 FDA reports)
SPONDYLOSIS ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 1 FDA reports)
STAPHYLOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STEAL SYNDROME ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
STIFF PERSON SYNDROME ( 1 FDA reports)
STOMACH MASS ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
STUBBORNNESS ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBDURAL EMPYEMA ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SULPHAEMOGLOBIN INCREASED ( 1 FDA reports)
SUNCT SYNDROME ( 1 FDA reports)
SUPPLEMENTATION THERAPY ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SUTURE REMOVAL ( 1 FDA reports)
SWEAT GLAND INFECTION ( 1 FDA reports)
SYNOSTOSIS ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TENODESIS ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR INJURY ( 1 FDA reports)
TESTICULAR NEOPLASM ( 1 FDA reports)
THALASSAEMIA TRAIT ( 1 FDA reports)
THERAPEUTIC AGENT URINE NEGATIVE ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THROMBOANGIITIS OBLITERANS ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THYROXINE ABNORMAL ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TOOTH DECALCIFICATION ( 1 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 1 FDA reports)
TRAUMATIC LIVER INJURY ( 1 FDA reports)
TRICHOPHYTOSIS ( 1 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TRIGEMINAL NERVE ABLATION ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
TRIGEMINAL NERVE INJECTION ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
TRYPTASE ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TURNER'S SYNDROME ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
TYPE II HYPERSENSITIVITY ( 1 FDA reports)
ULNAR NERVE PALSY ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UMBILICAL CORD VASCULAR DISORDER ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
UNWANTED AWARENESS DURING ANAESTHESIA ( 1 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERITIS ( 1 FDA reports)
URETHRAL INJURY ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINE DELTA AMINOLEVULINATE ( 1 FDA reports)
URINE OUTPUT ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
UROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UTERINE LEIOMYOSARCOMA ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VACTERL SYNDROME ( 1 FDA reports)
VAGINAL EROSION ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINAL NEOPLASM ( 1 FDA reports)
VARICOCELE ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULAR STENT INSERTION ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VASOPRESSIVE THERAPY ( 1 FDA reports)
VENIPUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENOUS PRESSURE JUGULAR ABNORMAL ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR DYSSYNCHRONY ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VICTIM OF ABUSE ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VICTIM OF ELDER ABUSE ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VICTIM OF SEXUAL ABUSE ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VIRAL SKIN INFECTION ( 1 FDA reports)
VIRUS URINE TEST POSITIVE ( 1 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 1 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
VITAMIN B1 INCREASED ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)
VITELLO-INTESTINAL DUCT REMNANT ( 1 FDA reports)
VITH NERVE DISORDER ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOCAL CORD CYST ( 1 FDA reports)
VOCAL CORD NEOPLASM ( 1 FDA reports)
VULVAL ABSCESS ( 1 FDA reports)
VULVAL NEOPLASM ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL DISORDER ( 1 FDA reports)
WAXY FLEXIBILITY ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WEIGHT BELOW NORMAL ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WINGED SCAPULA ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
YELLOW NAIL SYNDROME ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ABSCESS SWEAT GLAND ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACHOLIA ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACQUIRED CLAW TOE ( 1 FDA reports)
ACROCHORDON ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADENOSQUAMOUS CARCINOMA OF THE CERVIX ( 1 FDA reports)
ADENOVIRUS TEST POSITIVE ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADNEXA UTERI CYST ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 1 FDA reports)
ADVERSE EVENT FOLLOWING IMMUNISATION ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
AGRAPHIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
ALCOHOLIC SEIZURE ( 1 FDA reports)
ALLERGIC COUGH ( 1 FDA reports)
ALLERGIC OEDEMA ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ALLERGY TO PLANTS ( 1 FDA reports)
ALLERGY TO VACCINE ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN AMNIOTIC FLUID INCREASED ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMIMIA ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMOEBIASIS ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAL CANCER STAGE 0 ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANALGESIC DRUG LEVEL DECREASED ( 1 FDA reports)
ANDROGEN INSENSITIVITY SYNDROME ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANION GAP ABNORMAL ( 1 FDA reports)
ANOGENITAL DYSPLASIA ( 1 FDA reports)
ANOREXIA NERVOSA ( 1 FDA reports)
ANOTIA ( 1 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
AORTIC ANEURYSM REPAIR ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE DRYNESS ( 1 FDA reports)
APPLICATION SITE EXCORIATION ( 1 FDA reports)
APPLICATION SITE HAEMATOMA ( 1 FDA reports)
APPLICATION SITE HYPERAESTHESIA ( 1 FDA reports)
APPLICATION SITE INDURATION ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE ODOUR ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTHROPOD INFESTATION ( 1 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 1 FDA reports)
ARTIFICIAL MENOPAUSE ( 1 FDA reports)
ASCITES INFECTION ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 1 FDA reports)
ATHETOSIS ( 1 FDA reports)
ATLANTOAXIAL INSTABILITY ( 1 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
ATYPICAL FEMUR FRACTURE ( 1 FDA reports)
AURAL POLYP ( 1 FDA reports)
AURICULOTEMPORAL SYNDROME ( 1 FDA reports)
AUTOIMMUNE PANCREATITIS ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AUTOMATISM ( 1 FDA reports)
AUTOPHOBIA ( 1 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BACTERIAL ANTIGEN POSITIVE ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BARTHOLIN'S CYST REMOVAL ( 1 FDA reports)
BARTTER'S SYNDROME ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BASE EXCESS POSITIVE ( 1 FDA reports)
BASOPHIL COUNT INCREASED ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 1 FDA reports)
BETA GLOBULIN DECREASED ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BILIARY CANCER METASTATIC ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIARY TRACT OPERATION ( 1 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 1 FDA reports)
BIOPSY EYELID ( 1 FDA reports)
BIOPSY INTESTINE ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BIOPSY SKIN ( 1 FDA reports)
BISEXUALITY ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER PERFORATION ( 1 FDA reports)
BLEEDING TIME SHORTENED ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLINDNESS HYSTERICAL ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ALCOHOL ABNORMAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE ( 1 FDA reports)
BLOOD AMYLASE ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CALCITONIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CANNABINOIDS ( 1 FDA reports)
BLOOD CANNABINOIDS INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD ETHANOL DECREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD GASTRIN INCREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE DECREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD INSULIN ABNORMAL ( 1 FDA reports)
BLOOD INSULIN DECREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD IRON ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID ( 1 FDA reports)
BLOOD LACTIC ACID ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 1 FDA reports)
BLOOD PROLACTIN DECREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD SELENIUM DECREASED ( 1 FDA reports)
BLOOD THROMBOPLASTIN DECREASED ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE DENSITY ABNORMAL ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE SCAN ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BOWEL PREPARATION ( 1 FDA reports)
BRACHIAL PLEXUS LESION ( 1 FDA reports)
BRACHIOCEPHALIC VEIN STENOSIS ( 1 FDA reports)
BRADYCARDIA FOETAL ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN STEM AUDITORY EVOKED RESPONSE ABNORMAL ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST ADENOMA ( 1 FDA reports)
BREAST CYST EXCISION ( 1 FDA reports)
BREAST DISCOLOURATION ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREAST OEDEMA ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
BURGLARY VICTIM ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURN OF INTERNAL ORGANS ( 1 FDA reports)
BURNING FEET SYNDROME ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CALCIUM IONISED INCREASED ( 1 FDA reports)
CALLUS FORMATION DELAYED ( 1 FDA reports)
CAMPTODACTYLY CONGENITAL ( 1 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CAPSULE ISSUE ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 1 FDA reports)
CARBOHYDRATE TOLERANCE DECREASED ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARCINOID SYNDROME ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARCINOMA IN SITU ( 1 FDA reports)
CARCINOMA IN SITU OF SKIN ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC NEOPLASM MALIGNANT ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC REHABILITATION THERAPY ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOPULMONARY BYPASS ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CAROTID PULSE INCREASED ( 1 FDA reports)
CAROTID SINUS SYNDROME ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER SITE OEDEMA ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CAUTERY TO NOSE ( 1 FDA reports)
CD4 LYMPHOCYTES ABNORMAL ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CD4/CD8 RATIO DECREASED ( 1 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 1 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 1 FDA reports)
CEREBELLAR ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL DECOMPRESSION ( 1 FDA reports)
CEREBROSCLEROSIS ( 1 FDA reports)
CERUMEN REMOVAL ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CERVICAL ROOT PAIN ( 1 FDA reports)
CERVICECTOMY ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 1 FDA reports)
CHEMICAL BURN OF RESPIRATORY TRACT ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHOLELITHOTOMY ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CHONDROMATOSIS ( 1 FDA reports)
CHONDROSARCOMA ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COLON CANCER STAGE II ( 1 FDA reports)
COLON INJURY ( 1 FDA reports)
COLONIC HAEMATOMA ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COMA ACIDOTIC ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONGENITAL INGUINAL HERNIA ( 1 FDA reports)
CONGENITAL KYPHOSCOLIOSIS ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONTRACTED BLADDER ( 1 FDA reports)
CONTRAST MEDIA ALLERGY ( 1 FDA reports)
COPROPORPHYRINOGEN INCREASED ( 1 FDA reports)
CORNEAL EPITHELIUM DISORDER ( 1 FDA reports)
CORNEAL STAPHYLOMA ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIAL NERVE OPERATION ( 1 FDA reports)
CREATINE URINE DECREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CRIME ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF VOLUME INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CULTURE STOOL NEGATIVE ( 1 FDA reports)
CUTANEOUS LARVA MIGRANS ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYSTIC FIBROSIS LUNG ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
CYSTITIS RADIATION ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
CYTOGENETIC ANALYSIS ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DACRYOADENITIS ACQUIRED ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEATH OF CHILD ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DECREASED VIBRATORY SENSE ( 1 FDA reports)
DELAYED EFFECTS OF RADIATION ( 1 FDA reports)
DELAYED FONTANELLE CLOSURE ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DEVICE BATTERY ISSUE ( 1 FDA reports)
DEVICE DEPLOYMENT ISSUE ( 1 FDA reports)
DEVICE ELECTRICAL FINDING ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE INTERACTION ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC MACROANGIOPATHY ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIASTOLIC HYPOTENSION ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIZZINESS EXERTIONAL ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG HALF-LIFE REDUCED ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 1 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 1 FDA reports)
DRUG WITHDRAWAL MAINTENANCE THERAPY ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
EAR CANAL INJURY ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EAR LOBE INFECTION ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
EGOBRONCHOPHONY ( 1 FDA reports)
ELBOW OPERATION ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCUTION ( 1 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 1 FDA reports)
END STAGE AIDS ( 1 FDA reports)
ENDOCARDIAL FIBROELASTOSIS ( 1 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENDOTOXIC SHOCK ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROVIRUS TEST POSITIVE ( 1 FDA reports)
ENTROPION ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ERYTHROMELALGIA ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
ERYTHROSIS ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EXERTIONAL HEADACHE ( 1 FDA reports)
EXPANDED DISABILITY STATUS SCALE SCORE INCREASED ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTRINSIC VASCULAR COMPRESSION ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYEBALL RUPTURE ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELID TUMOUR ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FACIAL OPERATION ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FAECAL DISIMPACTION ( 1 FDA reports)
FAECAL ELASTASE CONCENTRATION DECREASED ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FALSE NEGATIVE LABORATORY RESULT ( 1 FDA reports)
FALSE POSITIVE TUBERCULOSIS TEST ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FEAR OF NEEDLES ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FIBRINOLYSIS INCREASED ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FLUORIDE INCREASED ( 1 FDA reports)
FOETAL CYSTIC HYGROMA ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GALLBLADDER CANCER METASTATIC ( 1 FDA reports)
GANGLION ( 1 FDA reports)
GANGLIONEUROMA ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC LAVAGE ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GENITAL DISCOMFORT ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GENITAL HYPOAESTHESIA ( 1 FDA reports)
GENITAL INFECTION ( 1 FDA reports)
GENITAL INFECTION VIRAL ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GINGIVAL GRAFT ( 1 FDA reports)
GINGIVAL INJURY ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLOSSOPHARYNGEAL NEURALGIA ( 1 FDA reports)
GLOTTIS CARCINOMA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GROWING PAINS ( 1 FDA reports)
GROWTH OF EYELASHES ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 1 FDA reports)
HAEMOPHILIA ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEAD BANGING ( 1 FDA reports)
HEARING DISABILITY ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEMIANOPIA HETERONYMOUS ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC HYDROTHORAX ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HEPATIC SIDEROSIS ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATIC VEIN OCCLUSION ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS C RNA ( 1 FDA reports)
HEPATITIS C RNA INCREASED ( 1 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HEPATOBLASTOMA ( 1 FDA reports)
HERNIA GANGRENOUS ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HIPPOCAMPAL SCLEROSIS ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOFFMANN'S SIGN ( 1 FDA reports)
HOOKWORM INFECTION ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUMAN T-CELL LYMPHOTROPIC VIRUS TYPE I INFECTION ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYDROCELE OPERATION ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 1 FDA reports)
HYPERCATABOLISM ( 1 FDA reports)
HYPERCHROMASIA ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPEREXPLEXIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 1 FDA reports)
HYPERINSULINISM ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERVITAMINOSIS ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOSOMNIA ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYSTEROSCOPY ( 1 FDA reports)
ICHTHYOSIS ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
IMMINENT ABORTION ( 1 FDA reports)
IMMUNE TOLERANCE INDUCTION ( 1 FDA reports)
IMMUNOLOGY TEST ( 1 FDA reports)
IMPAIRED REASONING ( 1 FDA reports)
IMPINGEMENT SYNDROME ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INFANT ( 1 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
INFESTATION ( 1 FDA reports)
INFUSION SITE ABSCESS ( 1 FDA reports)
INFUSION SITE IRRITATION ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INFUSION SITE THROMBOSIS ( 1 FDA reports)
INFUSION SITE WARMTH ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INGUINAL MASS ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE HYPERTROPHY ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INJECTION SITE RECALL REACTION ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 1 FDA reports)
INTELLIGENCE TEST ABNORMAL ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
INTESTINAL STOMA ( 1 FDA reports)
INTESTINAL STRANGULATION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
INVESTIGATION ( 1 FDA reports)
IRIS HYPOPIGMENTATION ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 1 FDA reports)
IRON METABOLISM DISORDER ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KERATORHEXIS ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
LARYNGEAL MASS ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LARYNGOTRACHEAL OPERATION ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEIOMYOSARCOMA METASTATIC ( 1 FDA reports)
LHERMITTE'S SIGN ( 1 FDA reports)
LIGAMENT CALCIFICATION ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIP NEOPLASM ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPIDS DECREASED ( 1 FDA reports)
LISTERIA SEPSIS ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LUMBAR PUNCTURE ( 1 FDA reports)
LUNG ADENOCARCINOMA RECURRENT ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 1 FDA reports)
LUNG INFILTRATION MALIGNANT ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPHADENITIS BACTERIAL ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MAGNESIUM DEFICIENCY ( 1 FDA reports)
MALE ORGASMIC DISORDER ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALIGNANT OLIGODENDROGLIOMA ( 1 FDA reports)
MARBURG'S VARIANT MULTIPLE SCLEROSIS ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MASTOPTOSIS ( 1 FDA reports)
MATERNAL DEATH AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEAN PLATELET VOLUME ABNORMAL ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MEDIASTINAL OPERATION ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEDICAL OBSERVATION ( 1 FDA reports)
MELANOMA RECURRENT ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENINGITIS HERPES ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENINGOCOCCAL SEPSIS ( 1 FDA reports)
MENINGOMYELOCELE ( 1 FDA reports)
MENTAL DISABILITY ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ADVANCED ( 1 FDA reports)
METABOLIC MYOPATHY ( 1 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 1 FDA reports)
METAPNEUMOVIRUS INFECTION ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASES TO SALIVARY GLAND ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
METASTASES TO SOFT TISSUE ( 1 FDA reports)
METASTASES TO THE MEDIASTINUM ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MIDDLE EAR DISORDER ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MIDDLE EAR INFLAMMATION ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MOUTH CYST ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MUNCHAUSEN'S SYNDROME ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCETOMA MYCOTIC ( 1 FDA reports)
MYCOBACTERIA TEST ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDIAL REPERFUSION INJURY ( 1 FDA reports)
MYOFASCIAL SPASM ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOKYMIA ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
NAIL PIGMENTATION ( 1 FDA reports)
NAIL PSORIASIS ( 1 FDA reports)
NARROW ANTERIOR CHAMBER ANGLE ( 1 FDA reports)
NASAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NASAL SEPTAL OPERATION ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECROTISING FASCIITIS STAPHYLOCOCCAL ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHROSTOMY ( 1 FDA reports)
NEPHROSTOMY TUBE REMOVAL ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROFIBROMATOSIS ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROMUSCULAR BLOCKADE ( 1 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 1 FDA reports)
NEUTRALISING ANTIBODIES NEGATIVE ( 1 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NEUTROPHIL COUNT ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NODAL OSTEOARTHRITIS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 1 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
OBSTETRIC PROCEDURE COMPLICATION ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCCUPATIONAL EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OCULOCEPHALOGYRIC REFLEX ABSENT ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPTIC NERVE CUPPING ( 1 FDA reports)
OPTIC NERVE HYPOPLASIA ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
ORAL BACTERIAL INFECTION ( 1 FDA reports)
ORAL HAIRY LEUKOPLAKIA ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
OROANTRAL FISTULA ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
ORTHOSTATIC TREMOR ( 1 FDA reports)
OSTEOPETROSIS ( 1 FDA reports)
OSTEOSARCOMA METASTATIC ( 1 FDA reports)
OVARIAN CANCER STAGE III ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OVERCONFIDENCE ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PALLIATIVE CARE ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREAS TRANSPLANT REJECTION ( 1 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 1 FDA reports)
PANCREATIC DUCT STENOSIS ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARASITE DNA TEST POSITIVE ( 1 FDA reports)
PARATHYROID REIMPLANTATION ( 1 FDA reports)
PARENT-CHILD PROBLEM ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PAST-POINTING ( 1 FDA reports)
PATIENT RESTRAINT ( 1 FDA reports)
PEDAL PULSE ABSENT ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PENILE EXFOLIATION ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERCUSSION TEST ABNORMAL ( 1 FDA reports)
PERIODONTAL OPERATION ( 1 FDA reports)
PERIPHERAL NERVE DESTRUCTION ( 1 FDA reports)
PERIPHERAL NERVE INFECTION ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERIPHERAL NERVE PALSY ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED STAGE IV ( 1 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 1 FDA reports)
PERITONEAL FIBROSIS ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PH URINE INCREASED ( 1 FDA reports)
PHARYNGEAL ABSCESS ( 1 FDA reports)
PHARYNGEAL CYST ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHARYNGEAL NEOPLASM ( 1 FDA reports)
PHOBIA OF DRIVING ( 1 FDA reports)
PHRENIC NERVE PARALYSIS ( 1 FDA reports)
PITUITARY ENLARGEMENT ( 1 FDA reports)
PLACENTA PRAEVIA ( 1 FDA reports)
PLATELET FACTOR 4 ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONECTOMY ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA ESCHERICHIA ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLIOMYELITIS ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYNEUROPATHY ALCOHOLIC ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POROKERATOSIS ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 1 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 1 FDA reports)
POSTERIOR INTEROSSEOUS SYNDROME ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 1 FDA reports)
POSTPARTUM DISORDER ( 1 FDA reports)
POUCHITIS ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PREGNANCY TEST POSITIVE ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY WITH INJECTABLE CONTRACEPTIVE ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PRODUCT SHAPE ISSUE ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PRODUCT USED FOR UNKNOWN INDICATION ( 1 FDA reports)
PROGRESSIVE RELAPSING MULTIPLE SCLEROSIS ( 1 FDA reports)
PROPHYLAXIS ( 1 FDA reports)
PROPIONIBACTERIUM INFECTION ( 1 FDA reports)
PROPOFOL INFUSION SYNDROME ( 1 FDA reports)
PROSTATE CANCER STAGE III ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROSTATIC DYSPLASIA ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN S ABNORMAL ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSITTACOSIS ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSYCHIATRIC EVALUATION ABNORMAL ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PSYCHOTHERAPY ( 1 FDA reports)
PUDENDAL CANAL SYNDROME ( 1 FDA reports)
PULMONARY AMYLOIDOSIS ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY HYPOPLASIA ( 1 FDA reports)
PULMONARY MALFORMATION ( 1 FDA reports)
PULMONARY RENAL SYNDROME ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY VALVE SCLEROSIS ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)